Quality Control Associate
Spectraforce
Matthews, North Carolina
a month ago
Job Description
Position Title: Quality Control Associate
Work Location: Holly Springs, NC, 27540
Assignment Duration: 12 Months
Work Schedule: Standard hours, up to 5 days per month may require shift flexibility
Work Arrangement: Fully Onsite
Position Summary: Lead and contribute to critical activities including system qualifications, method transfers, and laboratory operations in a GMP-regulated environment.
Key Responsibilities:
• Collaborate cross-functionally with site teams to implement work order and preventative maintenance systems for laboratory equipment.
• Review and contribute to validation documentation to support onboarding of equipment and computerized systems.
• Draft, revise, and review technical and quality documentation such as SOPs, test methods, technical assessments, validation reports, trend reports, and safety evaluations.
• Assist in the procurement of laboratory consumables and critical reagents required for startup activities.
• Coordinate and execute training and method transfer activities for instruments including HPLC, UPLC, TOC, and other chemistry-based platforms.
• Actively participate in audits, quality initiatives, and cross-functional projects with site or global impact.
• Provide routine operational support during weekends and public holidays as required.
Qualification & Experience:
• Bachelor’s degree or higher in Chemistry, Biochemistry, Chemical Engineering, Physics, or a related scientific discipline.
• Minimum of 4 years of relevant laboratory experience in a GMP pharmaceutical or biopharmaceutical manufacturing environment, with a strong background in analytical testing.
• Proficient in analytical laboratory techniques and instrumentation.
• Familiarity with laboratory systems such as LIMS and LMES/CIMS.
• Demonstrated understanding of industry regulations, data integrity, and compliance standards.
• Strong technical writing, documentation, and communication skills.
• Experience with method and equipment validation, including verification, transfer, and change control.
• Excellent interpersonal skills with the ability to collaborate across teams and adapt to varying communication styles.
• Ideal Candidate: B.S. and 1-3 YOE would be ideal in a chemistry lab environment.
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $29.00/hr.
Work Location: Holly Springs, NC, 27540
Assignment Duration: 12 Months
Work Schedule: Standard hours, up to 5 days per month may require shift flexibility
Work Arrangement: Fully Onsite
Position Summary: Lead and contribute to critical activities including system qualifications, method transfers, and laboratory operations in a GMP-regulated environment.
Key Responsibilities:
• Collaborate cross-functionally with site teams to implement work order and preventative maintenance systems for laboratory equipment.
• Review and contribute to validation documentation to support onboarding of equipment and computerized systems.
• Draft, revise, and review technical and quality documentation such as SOPs, test methods, technical assessments, validation reports, trend reports, and safety evaluations.
• Assist in the procurement of laboratory consumables and critical reagents required for startup activities.
• Coordinate and execute training and method transfer activities for instruments including HPLC, UPLC, TOC, and other chemistry-based platforms.
• Actively participate in audits, quality initiatives, and cross-functional projects with site or global impact.
• Provide routine operational support during weekends and public holidays as required.
Qualification & Experience:
• Bachelor’s degree or higher in Chemistry, Biochemistry, Chemical Engineering, Physics, or a related scientific discipline.
• Minimum of 4 years of relevant laboratory experience in a GMP pharmaceutical or biopharmaceutical manufacturing environment, with a strong background in analytical testing.
• Proficient in analytical laboratory techniques and instrumentation.
• Familiarity with laboratory systems such as LIMS and LMES/CIMS.
• Demonstrated understanding of industry regulations, data integrity, and compliance standards.
• Strong technical writing, documentation, and communication skills.
• Experience with method and equipment validation, including verification, transfer, and change control.
• Excellent interpersonal skills with the ability to collaborate across teams and adapt to varying communication styles.
• Ideal Candidate: B.S. and 1-3 YOE would be ideal in a chemistry lab environment.
Applicant Notices & Disclaimers
- For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $29.00/hr.