QC Analyst III Employment Type:
Contract To Hire Quality Control Operations Analyst III (Pharmaceutical/Biotech Industry Experience)
100% Onsite in Norton, MA
11 month contract with perm potential
Pay rate: $40 - $43.50 (depending on experience)
***Please note: This position is 1st Shift: Friday - Monday (4 x 10 hours), but will require an initial period of Monday-Friday work to accommodate training
***Requires 4 years' experience in a GMP Quality Control position along with executing routine and non-routine testing in support of development through commercial programs. This position will also play a role in method transfers, method qualification/validation, verification
and implementation.
Other Experience / Responsibilities:
- Perform routine and non-routine analytical and/or microbiological assays to support raw materials, in-process samples, product release, and stability studies, following established SOPs
- Support a continuous operational schedule by supporting weekend laboratory operations (Analytical, Microbiology, Raw Materials).
- Experience in method transfer and/or analytical method implementation; solid understanding of method lifecycle management and phase-appropriate approach is desirable
- Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics
- Demonstrated technical writing skills, with preference for technical writing of investigations/CAPAs
- Proficient in data analysis and interpretation, with excellent attention to detail to inform decision-making
- Perform role-specific operational assignments (e.g., raw material processes including SAP transactions, environmental monitoring, in-process testing, etc.).
- Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred
- Contribute to the revision and updating of controlled documents, including SOPs, work instructions, and test methods, to ensure continuous improvement and compliance with current industry standards and regulatory requirements
- Adhere to internal standards, policies, and SOPs, as well as regulatory and industry standards (e.g., GMP, GLP, ICH guidelines) to maintain the highest levels of quality and compliance.
- Participate in inspection readiness activities as well as supporting onsite audits and inspections, as needed.
- Collaborate with other organizational functions including CMC Development, Manufacturing, Manufacturing Technical Services, Materials Management, and Quality Assurance to ensure alignment with overall business goals.
EDUCATION: B.S. in chemistry, biology, or biochemistry, or related scientific field;
Estimated Min Rate: $40.00
Estimated Max Rate: $43.50
Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Visit
https://www.yoh.com/applicants-with-disabilities
to contact us if you are an individual with a disability and require accommodation in the application process.
For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
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YOH Services LLC
Jan 16, 2025