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Sr. Quality Control Analyst
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Scorecard
Based on Massachusetts data
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What they do
A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
$75,723 / year median in Massachusetts
-9% projected decline
Job Description
- 2.7 Waltham, MA Job Details Full-time $105,000
- $120,000 a year 10 hours ago Benefits Wellness program Health savings account Paid holidays Health insurance Dental insurance 401(k) Flexible spending account Tuition reimbursement Paid time off Parental leave Employee assistance program Vision insurance Qualifications Content creation for technical audiences Team leadership Technical documentation Technical writing experience within manufacturing Microsoft Office Policy & process development Laboratory standard operating procedures Leading team collaboration initiatives Managing projects GMP for research safety and compliance Project leadership Standard operating procedures (SOPs) Project planning phase Technical Proficiency Standard operating procedures drafting Drug formulation
Full Job Description Shift:
Monday through Friday, 8:00AM- 5:00PM Are you ready to work making the world a safer, healthier place?
Description:
Lead formulation and process development for innovative drug products. Provide expert guidance on material and product evaluation using advanced technical knowledge. Design scalable formulations for small molecules and biologics in early-stage clinical trials. Optimize manufacturing processes and interpret analytical data to drive strategic decisions.Compensation:
$105,000.00- 120,000.
Responsibilities:
Analyze and interpret complex chemistry, biochemistry, and formulation data to identify trends and provide actionable insights to management and/or clients. Develop, validate, and transfer analytical methods; perform routine and advanced testing using instruments such as HPLC, GC, LC-MS, FTIR, and ddPCR. Design and develop robust, scalable formulations for small molecules and biologics in early-stage clinical trials; optimize manufacturing processes for drug products. Write and review GMP SOPs Conduct analytical testing following SOPs, regulatory guidelines, and GMP standards. Train and mentor team members on analytical methods, instrumentation, and best practices, as required Collaborate across teams to improve efficiency and deliver high-quality results. Promote a positive, customer-focused environment aligned with Pace®'s mission.Requirements:
Education:
Bachelor's, Master's, or PhD degree in Chemistry, Biology, or a related field (advanced degree preferred).Experience:
5+ years in a laboratory setting with demonstrated expertise in analytical methods and formulation development. 3+ years of technical writing experience, including GMP SOP development.Skills:
Strong organizational, leadership, and communication abilities. Ability to manage multiple projects simultaneously; self-motivated and results-driven. Proficiency with Office 365 and laboratory instrument software Independent in time management and project planningMindset:
Collaborative, detail-oriented, and committed to quality and compliance. Find Your Place at Pace- We need you
- your curiosity, your talents, and your drive
- to help us advance this important work.