4 jobs found in collegeville, pennsylvania

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    • collegeville, pennsylvania
    • contract
    • US$54.46 - US$64.08, per hour, $54.46 - 64.08 per hour
    • 9 to 5
    job summary:As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now! location: Collegeville, Pennsylvaniajob type: Contractsalary: $54.46 - 64.08 per hourwork hours: 9 to 5education: Bachelors responsibilities:Seeking a highly skilled scientist with a demonstrated track record of applying knowledge to the introduction of innovative solutions in the area of microbiology testing. This is an exciting and unique role where the applicant will have the opportunity to evaluate novel microbiology methods for testing chemical and biological products. The successful applicant will focus on the development and validation of transformational microbiology methodologies, driving execution of proof of concept studies, validation and implementation into biological and pharmaceutical products and processes.Key responsibilities:- Seek rapid/alternative microbiological technologies for microbiological tests (such automated colony counters and rapid bioburden, sterility, mycoplasma and adventitious viral agent assays).- Review the technologies and advise on their feasibility.- Design and execute proof of concept studies for new rapid microbiology technologies.- Execute method development and GMP validation for the rapid methods.- Provide validation and testing data for the new method for internal advocacy and external regulatory submission.- Maintain training records and familiarity with applicable SOPs and controlled documents- Work to GMP standards as appropriate.- Follow safe Laboratory Practices, regular safety training, and maintain accurate and complete safety records consistent with company policy and legal requirements. qualifications:- BSc in Microbiology or a related subject.- An understanding of the theoretical and practical aspects of Pharmaceutical Microbiology (knowledge of rapid/alternative methodologies an advantage)- Demonstrated hands-on and/or practical experience in microbiological analysis of pharmaceutical products - 2-5 years exp.- Able to provide original thinking for microbiology methodology development, with particular focus on novel on line and off line microbiology testing.- Experience with GMP laboratory operations and FDA regulations- Strong team working skills, able to effectively work across interdisciplinary groups- Capacity to think innovatively and flexibly, comfortable with complexity- Strong desire to learn/scientific curiosity, with cross functional learning agility- Good organizational skills and ability to multi task- Excellent verbal and written communication- Self-motivationPreferred Qualifications:- Experience with molecular techniques such as qPCR and NexGen sequencing.- Experience in microbiology method development/validation in pharmaceutical products.- Knowledge of pharmaceutical environmental and manufacturing microbiology. skills: MicrobiologyEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    job summary:As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now! location: Collegeville, Pennsylvaniajob type: Contractsalary: $54.46 - 64.08 per hourwork hours: 9 to 5education: Bachelors responsibilities:Seeking a highly skilled scientist with a demonstrated track record of applying knowledge to the introduction of innovative solutions in the area of microbiology testing. This is an exciting and unique role where the applicant will have the opportunity to evaluate novel microbiology methods for testing chemical and biological products. The successful applicant will focus on the development and validation of transformational microbiology methodologies, driving execution of proof of concept studies, validation and implementation into biological and pharmaceutical products and processes.Key responsibilities:- Seek rapid/alternative microbiological technologies for microbiological tests (such automated colony counters and rapid bioburden, sterility, mycoplasma and adventitious viral agent assays).- Review the technologies and advise on their feasibility.- Design and execute proof of concept studies for new rapid microbiology technologies.- Execute method development and GMP validation for the rapid methods.- Provide validation and testing data for the new method for internal advocacy and external regulatory submission.- Maintain training records and familiarity with applicable SOPs and controlled documents- Work to GMP standards as appropriate.- Follow safe Laboratory Practices, regular safety training, and maintain accurate and complete safety records consistent with company policy and legal requirements. qualifications:- BSc in Microbiology or a related subject.- An understanding of the theoretical and practical aspects of Pharmaceutical Microbiology (knowledge of rapid/alternative methodologies an advantage)- Demonstrated hands-on and/or practical experience in microbiological analysis of pharmaceutical products - 2-5 years exp.- Able to provide original thinking for microbiology methodology development, with particular focus on novel on line and off line microbiology testing.- Experience with GMP laboratory operations and FDA regulations- Strong team working skills, able to effectively work across interdisciplinary groups- Capacity to think innovatively and flexibly, comfortable with complexity- Strong desire to learn/scientific curiosity, with cross functional learning agility- Good organizational skills and ability to multi task- Excellent verbal and written communication- Self-motivationPreferred Qualifications:- Experience with molecular techniques such as qPCR and NexGen sequencing.- Experience in microbiology method development/validation in pharmaceutical products.- Knowledge of pharmaceutical environmental and manufacturing microbiology. skills: MicrobiologyEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    • collegeville, pennsylvania
    • contract
    • US$24.06 - US$28.31, per hour, $24.06 - 28.31 per hour
    • 9 to 5
    job summary:As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now! location: Collegeville, Pennsylvaniajob type: Contractsalary: $24.06 - 28.31 per hourwork hours: 9 to 5education: High School responsibilities:? With minimal supervision, perform manufacturing operations in chemical R&D pilot plants (e.g. operate equipment and processing areas), in order to develop chemical processes and prepare chemical supplies for R&D studies.? Assist in the maintenance of chemical R&D pilot plant equipment and processing areas, so that the facilities are in a continual state of readiness.? As required, assist in Installation Qualifications, Operational Qualifications, and Process Qualifications in order to keep the pilot plant facilities qualified.? Follow operating instructions and maintain accurate records as required to ensure the successful preparation of chemical supplies.? Perform all manufacturing operations according to the Safety, Environmental, and GMP guidelines followed by .? Assist in the materials management program within the chemical R&D pilot plants, in order to keep raw material and spare part inventories at their proper levels, to ensure that materials are properly staged and labeled, to ensure that waste is properly disposed, and to ensure that appropriate records are maintained.? Suggest improvements to equipment and operating procedures in order to successfully transfer lab-scale processes into the pilot plant facilities.? Communicate in an accurate and timely manner with subordinates, peers, and supervisors as required to successfully achieve project goals.? Provide training as necessary to less experienced operators.? Attend training courses as required qualifications:We are looking for professionals with these required skills to achieve our goals:? 3 years of experience in the chemical or pharmaceutical industry as an operator.? Excellent knowledge of chemical pilot plant operations, preferably as performed in the pharmaceutical industry.? Strong mechanical aptitude.? Must be able to work independently and as a member of a team with other plant operators, supervisors, chemists, and maintenance personnel.? Must be self-motivated.? Must be able to communicate effectively? Must be able to work shift work.? Must be able to lift over fifty pounds.? Must be able to move drums weighing 400 to 600 lbs. using the equipment available.Preferred Qualifications: If you have the following characteristics, it would be a plus:? 5 years of experience in the fine chemicals or pharmaceutical industry? 1 year of experience in chemical pilot plant operations? A good understanding of the safety, environmental, and GMP regulations (as applied to primary pharmaceutical manufacturing) skills: GMP (Good Manufacturing Practice)Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    job summary:As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now! location: Collegeville, Pennsylvaniajob type: Contractsalary: $24.06 - 28.31 per hourwork hours: 9 to 5education: High School responsibilities:? With minimal supervision, perform manufacturing operations in chemical R&D pilot plants (e.g. operate equipment and processing areas), in order to develop chemical processes and prepare chemical supplies for R&D studies.? Assist in the maintenance of chemical R&D pilot plant equipment and processing areas, so that the facilities are in a continual state of readiness.? As required, assist in Installation Qualifications, Operational Qualifications, and Process Qualifications in order to keep the pilot plant facilities qualified.? Follow operating instructions and maintain accurate records as required to ensure the successful preparation of chemical supplies.? Perform all manufacturing operations according to the Safety, Environmental, and GMP guidelines followed by .? Assist in the materials management program within the chemical R&D pilot plants, in order to keep raw material and spare part inventories at their proper levels, to ensure that materials are properly staged and labeled, to ensure that waste is properly disposed, and to ensure that appropriate records are maintained.? Suggest improvements to equipment and operating procedures in order to successfully transfer lab-scale processes into the pilot plant facilities.? Communicate in an accurate and timely manner with subordinates, peers, and supervisors as required to successfully achieve project goals.? Provide training as necessary to less experienced operators.? Attend training courses as required qualifications:We are looking for professionals with these required skills to achieve our goals:? 3 years of experience in the chemical or pharmaceutical industry as an operator.? Excellent knowledge of chemical pilot plant operations, preferably as performed in the pharmaceutical industry.? Strong mechanical aptitude.? Must be able to work independently and as a member of a team with other plant operators, supervisors, chemists, and maintenance personnel.? Must be self-motivated.? Must be able to communicate effectively? Must be able to work shift work.? Must be able to lift over fifty pounds.? Must be able to move drums weighing 400 to 600 lbs. using the equipment available.Preferred Qualifications: If you have the following characteristics, it would be a plus:? 5 years of experience in the fine chemicals or pharmaceutical industry? 1 year of experience in chemical pilot plant operations? A good understanding of the safety, environmental, and GMP regulations (as applied to primary pharmaceutical manufacturing) skills: GMP (Good Manufacturing Practice)Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    • collegeville, pennsylvania
    • contract
    • US$76.34 - US$89.82, per hour, $76.34 - 89.82 per hour
    • 9 to 5
    job summary:As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now! location: Collegeville, Pennsylvaniajob type: Contractsalary: $76.34 - 89.82 per hourwork hours: 9 to 5education: Bachelors responsibilities:- Support EMU Biomarker and Companion Diagnostic Teams in the delivery of clinical biomarker, companion diagnostic and translational research objectives by leading cross-functional project teams; coordinate activities across Clinical Development, Clinical Operations, Data Management, Quality, Regulatory, Procurement, Finance, Commercial, etc.- Work closely with internal cross-functional project teams and external partners (e.g. analytical labs, diagnostic manufacturers, academic collaborators, etc.) to ensure that project objectives are delivered according to agreed scope, cost, quality and timeline milestones- Analyze, plan, and track project activities; identify and resolve operational problems and minimize delays- Communicate timelines, milestones and goals on a routine basis to Biomarker and Companion Diagnostic Leads, the project team and other stakeholders- Identify and communicate risks to timeline, budget, scope, etc. to stakeholders in a timely and clear manner- Manage vendor contracts and approval of invoices- Track and update project budgets, milestones and payments- Organize internal scientific/strategy meetings as well as meetings with external partners (e.g. Joint Project Team meetings, F2F meetings, etc.), provide expert records of discussions, and ensure timely resolution of actions- Enable Subject Matter Expert driven support to programs by demonstrating a broad knowledge of biomarker and companion diagnostic technologies and IVD development- Successfully multi-task amongst several competing initiatives- Demonstrate accountability and urgency for the timely completion of EMU projects qualifications:- Bachelor's degree in biological sciences or related discipline; advanced scientific degree a plus- Minimum of 5 years of project or program management experience in the diagnostic, pharmaceutical, or biotech industry- Understanding of drug discovery and development, clinical trial design, and overall principles of clinical development- Knowledge and experience in both companion diagnostic and pharmaceutical development, analytical and clinical validations, and regulatory submissions a plus- Good understanding and application of Project Management principles, concepts, practices and standards; PMP certification a plus- Established expertise and hands-on experience with Microsoft Project or equivalent, Word, Excel, PowerPoint, Outlook, SharePoint and remote meeting tools such as MS Teams, WebEx, etc.EXPERTISE & SKILLS:- Demonstrated ability to think strategically, work effectively in a matrixed environment, and execute multiple projects simultaneously- Excellent time management skills, well organized, and focused on results- Ability to establish trust and work with integrity while motivating others to achieve the goals of the project- Highly effective communication skills (verbal, written, and presentation) and negotiation skills for a wide variety of audiences/stakeholders, including technical and business skills: PMPEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    job summary:As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now! location: Collegeville, Pennsylvaniajob type: Contractsalary: $76.34 - 89.82 per hourwork hours: 9 to 5education: Bachelors responsibilities:- Support EMU Biomarker and Companion Diagnostic Teams in the delivery of clinical biomarker, companion diagnostic and translational research objectives by leading cross-functional project teams; coordinate activities across Clinical Development, Clinical Operations, Data Management, Quality, Regulatory, Procurement, Finance, Commercial, etc.- Work closely with internal cross-functional project teams and external partners (e.g. analytical labs, diagnostic manufacturers, academic collaborators, etc.) to ensure that project objectives are delivered according to agreed scope, cost, quality and timeline milestones- Analyze, plan, and track project activities; identify and resolve operational problems and minimize delays- Communicate timelines, milestones and goals on a routine basis to Biomarker and Companion Diagnostic Leads, the project team and other stakeholders- Identify and communicate risks to timeline, budget, scope, etc. to stakeholders in a timely and clear manner- Manage vendor contracts and approval of invoices- Track and update project budgets, milestones and payments- Organize internal scientific/strategy meetings as well as meetings with external partners (e.g. Joint Project Team meetings, F2F meetings, etc.), provide expert records of discussions, and ensure timely resolution of actions- Enable Subject Matter Expert driven support to programs by demonstrating a broad knowledge of biomarker and companion diagnostic technologies and IVD development- Successfully multi-task amongst several competing initiatives- Demonstrate accountability and urgency for the timely completion of EMU projects qualifications:- Bachelor's degree in biological sciences or related discipline; advanced scientific degree a plus- Minimum of 5 years of project or program management experience in the diagnostic, pharmaceutical, or biotech industry- Understanding of drug discovery and development, clinical trial design, and overall principles of clinical development- Knowledge and experience in both companion diagnostic and pharmaceutical development, analytical and clinical validations, and regulatory submissions a plus- Good understanding and application of Project Management principles, concepts, practices and standards; PMP certification a plus- Established expertise and hands-on experience with Microsoft Project or equivalent, Word, Excel, PowerPoint, Outlook, SharePoint and remote meeting tools such as MS Teams, WebEx, etc.EXPERTISE & SKILLS:- Demonstrated ability to think strategically, work effectively in a matrixed environment, and execute multiple projects simultaneously- Excellent time management skills, well organized, and focused on results- Ability to establish trust and work with integrity while motivating others to achieve the goals of the project- Highly effective communication skills (verbal, written, and presentation) and negotiation skills for a wide variety of audiences/stakeholders, including technical and business skills: PMPEqual Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    • collegeville, pennsylvania
    • contract
    • US$42.29 - US$49.76, per hour, $42.29 - 49.76 per hour
    • 9 to 5
    job summary:As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now! location: Collegeville, Pennsylvaniajob type: Contractsalary: $42.29 - 49.76 per hourwork hours: 9 to 5education: Bachelors responsibilities:Requirements include being well grounded in a scientific discipline performing routine and complex bench and/or instrumental analysis. Must have good troubleshooting capabilities and able to develop methods and procedures. Must interpret and analyze data. positions work under direct supervision of a group leader, project manager, or lab manager. Must have very strong written and oral communication skills and be computer literate. Must have B.S. or M.S. degree or equivalent in a science. 5 or more years of work experience required. qualifications:Basic Qualifications:-BS or MS degree in Biology, Biochemistry, Analytical Chemistry, Molecular Biology, Immunology or a related scientific field.- Expertise in molecular biology and immunoassay development- 3-6+ years of post-graduate experience with at least 2+ years' experience with one of the following biochemical techniques: ELISA, qPCR, SDS-PAGE, 2-D DIGE, or Western blot.-Experience with computer software packages such as Excel, Word and PowerPoint is required.-Excellent communication and writing skills.- Ability to design, develop and qualify analytical methods based on biochemical and/or immunological methodologies with minimal supervision.Preferred Qualifications:- Proficiency with most of the following biochemical techniques, including: ELISA, quantitative PCR, SDS-PAGE, 2-D DIGE, and Western blot is preferred.- A strong background in immunological assay development, with demonstrated ability to assess and implement novel analytical technologies.- Understanding of biopharmaceutical upstream and downstream process development.- Practical experience with laboratory automation, specifically regarding programming liquid handling systems.- Knowledge of statistical methods as applied to bioanalytical data interpretation is preferred. skills: PCR, GMP (Good Manufacturing Practice)Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    job summary:As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team now! location: Collegeville, Pennsylvaniajob type: Contractsalary: $42.29 - 49.76 per hourwork hours: 9 to 5education: Bachelors responsibilities:Requirements include being well grounded in a scientific discipline performing routine and complex bench and/or instrumental analysis. Must have good troubleshooting capabilities and able to develop methods and procedures. Must interpret and analyze data. positions work under direct supervision of a group leader, project manager, or lab manager. Must have very strong written and oral communication skills and be computer literate. Must have B.S. or M.S. degree or equivalent in a science. 5 or more years of work experience required. qualifications:Basic Qualifications:-BS or MS degree in Biology, Biochemistry, Analytical Chemistry, Molecular Biology, Immunology or a related scientific field.- Expertise in molecular biology and immunoassay development- 3-6+ years of post-graduate experience with at least 2+ years' experience with one of the following biochemical techniques: ELISA, qPCR, SDS-PAGE, 2-D DIGE, or Western blot.-Experience with computer software packages such as Excel, Word and PowerPoint is required.-Excellent communication and writing skills.- Ability to design, develop and qualify analytical methods based on biochemical and/or immunological methodologies with minimal supervision.Preferred Qualifications:- Proficiency with most of the following biochemical techniques, including: ELISA, quantitative PCR, SDS-PAGE, 2-D DIGE, and Western blot is preferred.- A strong background in immunological assay development, with demonstrated ability to assess and implement novel analytical technologies.- Understanding of biopharmaceutical upstream and downstream process development.- Practical experience with laboratory automation, specifically regarding programming liquid handling systems.- Knowledge of statistical methods as applied to bioanalytical data interpretation is preferred. skills: PCR, GMP (Good Manufacturing Practice)Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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