QC Chemistry Associate I

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

Job Overview

Entry level position, individual contributor responsible for conducting routine analysis of raw materials, proteins, peptides and small molecules under general supervision for in-process, release and stability testing. May focus on a specialized area and provide routine analysis and testing according to standard operating procedures in any of the following areas: raw materials, in-process, and finished formulations.

Essential Duties And Responsibilities

• Perform routine analysis and testing in a GMP environment (including compendial assays, AQL inspections, and USP identification test methods, ensuring compliance with industry standards.
• May participate in qualification/verification of assays
• Perform Assay and documentation review.
• Writes and reviews product specifications as required.
• Collects and disposes of lab waste according to established procedures.
• Contribute to lab readiness including lab cleaning, glass washing, and inventory management
• Maintain personal training records. Attend all required training.
• Regular and reliable attendance on a full-time basis [or in accordance with posted schedule].
• Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
• Embodies PCI Pharma’s cultural values and aligns daily actions with department goals and company culture.
  
  

Qualifications

• High School Diploma required. Bachelor’s degree in Life Sciences discipline or equivalent preferred.
• Minimum of zero to two years of relevant work experience
• Ability to perform testing in a highly accurate and reproducible manner
• Follow GMP guidelines and detailed direction in a laboratory environment
• Familiarity with cGMP, manufacturing, instrument operations, troubleshooting and data entry
• Strong communication and teamwork
• Needs regular supervision to deliver goals and objectives
  
  

The hiring rate for this position is $26.73 - $27.00/hour plus eligibility for an annual performance bonus. Final offer amounts are determined by multiple factors including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), flexible spending account, and 401(k).

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement

PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.