Quality Control Analyst I
- Contract
- Good Manufacturing Practice (GMP)
- United States
This vacancy has now expired. Please see similar roles below...
Quality Control Analyst I -Contract - Norton, MA
Proclinical is seeking a Quality Control Analyst I for a contract role in Norton, MA.
Primary Responsibilities:
This position focuses on performing various operational assignments and analytical assays to support quality control activities. The successful candidate will need attention to detail, adherence to schedules, and collaboration with cross-functional teams.
Skills & Requirements:
- Experience in environmental monitoring and critical utility sampling.
- Proficiency in performing analytical and microbiological assays.
- Strong organizational skills and ability to maintain accurate training records.
- Familiarity with laboratory equipment maintenance and inventory management.
- Ability to ensure timely data submission and review.
- Experience in revising and updating controlled documents.
- Knowledge of GMP, GLP, and ICH guidelines.
- Effective collaboration and communication skills.
- Experience in inspection readiness and supporting audits.
- Commitment to continuous improvement in QC processes.
The Quality Control Analyst I responsibilities will be:
- Conduct environmental monitoring and critical utility sampling in cleanroom spaces.
- Perform routine and non-routine analytical and microbiological assays for raw materials, in-process samples, product release, and stability studies.
- Maintain training records, adhere to testing schedules, and ensure timely completion of assignments.
- Assist in maintaining laboratory equipment and inventory, including reagent and sample preparation.
- Ensure timely data submission and may qualify as a data reviewer.
- Contribute to the revision and updating of controlled documents, including SOPs and test methods.
- Adhere to internal standards, policies, SOPs, and regulatory guidelines (e.g., GMP, GLP, ICH).
- Collaborate with QC and cross-functional teams to support quality control operations.
- Participate in inspection readiness activities and support onsite audits and inspections.
- Support continuous improvement initiatives to enhance QC processes and laboratory efficiency.
If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at A.Maldonado@Proclinical.com
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
INDCQA
Related jobs
Highly Competitive
Göttingen, Germany
Proclinical sucht für ein Pharmaunternehmen einen Laborant (m/w/d) QC.
Highly Competitive
Philadelphia, USA
Proclinical is partnered with a pharmaceutical company seeking a QA Raw Materials Supervisor for a role in Philadelphia, PA.
Highly Competitive
Philadelphia, USA
Proclinical is working alongside a pharmaceutical company seeking a QA Release Supervisor, Cell Therapy to join their team!
Highly Competitive
Philadelphia, USA
Proclinical is seeking a highly motivated QA Specialist II to join the Quality Operations team for a night shift role.
Highly Competitive
Cambridge, England
Proclinical is currently working alongside a consultancy company to recruit for a Head of Quality & Operations. This is a permanent position based in Cambridge, United Kingdom.
Highly Competitive
Stein, Switzerland
Proclinical is currently working alongside a Contract Manufacturing Organisation to recruit for a Swiss Commissioning Engineer. This is a temporary contract position based in Stein, Switzerland.