Microbiologist I, EM - Framingham

The Environmental Monitoring Microbiologist conducts cleanroom monitoring activities to ensure the air, surfaces, and critical utilities utilized for pharmaceutical product manufacturing meet cGMP requirements. · ...

The main objective of the microbiologist shall be to ensure that quality central conforms to the standards of the European and United States Pharmacopoeias and the good manufacturing practice (GMP), the analytical methods used are appropriate and validated and that the results ob ...

Performs lab testing and associated activities within the Microbiology section. · Troubleshoots and maintains the LIS and instruments interface and software. · Resolves client problems as needed. · ...

Perform bioburden method qualification of raw material, in-process, and bulk drug substance samples. · Perform routine bioburden and endotoxin testing in accordance with SOPs, safety, and cGMP guidelines to support the release of finished products, · ...

Searching for a highly motivated individual with microbiological experience to work in quality control laboratory. · ...

Perform bioburden and endotoxin testing in accordance with SOPs. · ...

+Biohazardous Agent work quality: Able to perform tasks accurately and consistently; willing to speak up if more training is required; able to catch mistakes and bring them to the team's attention. · +Minimum of 1 - 2 years of experience in biopharmaceutical industry, preferably ...

Mindlance partners with leading employers across the country. Seeking Microbiologist with biopharmaceutical experience in quality control microbiology laboratory. · ...

Perform bioburden method qualification of raw material. Testing · Pate Reading · Organism Preparation · Result Tracking and Assay Review. ...

Job Description: Perform routine utility sampling and in-process testing, monitor equipment parameters, coordinate sample receipt and storage. Qualifications: B.S. in biological sciences or equivalent, 0-2 years of experience in regulated microbiology laboratory. · ...

We are looking for an experienced Clinical Microbiologist to join our Science & Clinical team on a part-time basis. This is a high-impact moment to join a small, mission-driven company working on technology that will fundamentally change how the world detects invisible threats. · ...

We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, · The Patient-centric And Award-winning Approach We're Taking In Business Fuels Our focus on science and innovation, · a commitment to developing and comm ...

We See You. · Your wellbeing · Your professional worth · Your future at EyePoint · ...

This role will be responsible for the review of GMP documentation respective to QC Microbiology assay and activities. · ...

Perform GMP testing of raw materials, in-process and finished products, stability samples, and non-routine sample analyses per established procedures and methodology. · ...

This is an on-site role in Norton, MA, with occasional responsibilities at other client locations. Weekend coverage is required.The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commer ...

At Client we are creating innovative medicines for patients who are fighting serious diseases. We are also nurturing our own team with inspiring work and challenging career options. · Perform routine environmental monitoring and clean utilities sampling and testing in accordance ...

Responsible for all microbiological and some analytical testing of production materials under GMP conditions. · ...

+Job summary · The Quality Control Operations Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. · +QualificationsB.S. in chemistry, biology, biochemistry or related field · 4-8 years of pharmaceutical/b ...

Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs. · ...