A Laboratory Analyst opportunity is available in Arecibo, PR with a leading organization in the pharmaceutical industry. This temp-to-hire role is ideal for a detail-oriented science professional who enjoys analytical testing, quality control, laboratory documentation, and working in a regulated GMP environment. The Laboratory Analyst will support critical laboratory operations by testing raw materials, in-process samples, and finished products to help ensure product quality, safety, and compliance. This is a strong opportunity to build a career in a stable, quality-focused manufacturing environment with supportive leadership, collaborative teams, and exposure to regulated laboratory processes. Candidates can expect a professional setting where accuracy, teamwork, training, and continuous improvement are valued. Required Qualifications and Skills:
Key Responsibilities:
- Perform routine and non-routine laboratory testing of raw materials, in-process samples, and finished products.
- Conduct chemical, physical, and analytical testing according to approved methods, specifications, SOPs, and regulatory requirements.
- Operate, calibrate, and maintain laboratory instruments and analytical equipment such as HPLC, GC, UV-Vis, FTIR, and pH meters.
- Review, document, interpret, and report analytical results while maintaining accurate GMP and GDP laboratory records.
- Support laboratory investigations, deviations, OOS results, CAPA activities, method validation, and continuous improvement initiatives.
- Collaborate with Quality Assurance, Manufacturing, Engineering, and other cross-functional teams to support quality and operational needs.
- Bachelor’s degree in Chemistry, Chemical process, Biology, Microbiology, Biotechnology, Chemical Sciences.
- 1 to 2 years of relevant laboratory, analytical testing, quality control, or laboratory operations experience preferred.
- Knowledge of GMP, GLP, GDP, SOPs, laboratory safety procedures, and regulated laboratory practices.
- Familiarity with analytical testing techniques and laboratory instrumentation, including HPLC, GC, UV-Vis, FTIR, pH measurement, and related methods.
- Ability to interpret laboratory data, follow technical procedures, and maintain clear, accurate documentation.
- Strong analytical thinking, organization, time management, problem-solving, and attention to detail.
- Ability to work independently and collaboratively with Quality, Manufacturing, Engineering, and laboratory teams.
Preferred Qualifications:
- Experience in pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
- Prior hands-on experience with HPLC, GC, UV-Vis, FTIR, and other quality control laboratory instruments.
Equal Opportunity Employer / Disabled / Protected Veterans
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