Global Leader In Life Sciences Talent Solutions
Planet Pharma stands as a global leader in life sciences recruitment and staffing, connecting exceptional talent with groundbreaking organizations across pharmaceuticals, biotechnology, medical devices, clinical research organizations, and healthcare labs. Founded in 2012 and headquartered in Raleigh, North Carolina, this rapidly growing company has expanded to over 1,000 employees across offices in North America, Europe, and APAC, establishing itself as a trusted partner in advancing health and science innovation.
Comprehensive Life Sciences Solutions
Planet Pharma specializes in contract and direct hire staffing, strategic resourcing, retained and executive search, Functional Service Provider (FSP) solutions, and global workforce solutions. The company's deep technical expertise and industry knowledge enable them to support complex projects requiring specialized skills in downstream process development, analytical chemistry, CMC biologics, and advanced data management. Their commitment to leveraging cutting-edge technology and flexible service delivery models ensures personalized solutions that exceed client and candidate expectations.
Technical Excellence and Professional Development
- Access to cutting-edge projects with leading biotechnology and pharmaceutical companies
- Opportunities across diverse life sciences sectors including CMOs/CDMOs and specialty providers
- Technical roles supporting biologics development, process development, and regulatory compliance
- Global career opportunities with offices spanning multiple continents
- Collaborative work environment with cross-functional teams and decision-makers at the table
- Full-time laboratory work with state-of-the-art equipment and hands-on technical development
Company Culture and Values
At Planet Pharma, decision-makers are at the table with the tools and expertise to create enduring, valuable relationships. The company strengthens the employer-employee dynamic by connecting clients with talent and making staffing more personal. With a highly technical approach and emphasis on scientific rigor and regulatory compliance, Planet Pharma offers professionals the opportunity to contribute to groundbreaking health and science innovations while working in a supportive environment that values technical excellence, independent problem-solving, and collaborative teamwork.
Mission
Support groundbreaking advancements in health and science by ensuring every step forward is backed by the expertise, passion, and commitment of top-tier life sciences professionals.
Frequently Asked Questions
Jobs for Planet Pharma in United States
17 results
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Planet Pharma$31/hr - $33/hr27540 Holly Springs, NC
Planet Pharma$75K/yr - $80K/yrConcord, OH
Planet Pharma$34/hr91362 Thousand Oaks, CA
Planet Pharma04074 Scarborough, ME
Planet Pharma30604 Athens, GA
Planet Pharma95828 Sacramento, CA
Planet Pharma37621 Bristol, TN
Planet Pharma15289 Pittsburgh, PA
Planet Pharma60086 North Chicago, IL
Planet Pharma92713 Irvine, CA
Planet Pharma$25/hr - $26/hr65231 Auxvasse, MO
Planet PharmaMiramar, FL
Planet Pharma94083 South San Francisco, CA
Planet Pharma$45/hr - $65/hr94061 Redwood City, CA
Planet Pharma$45/hr - $55/hr94061 Redwood City, CA
Planet Pharma$23/hr - $25/hr84193 Salt Lake City, UT
Planet Pharma$28/hr - $32/hr92189 San Diego, CA

Sr. Quality Assurance Associate Plant Quality Assurance
Description
Pay $31-$33 per hr.
Fully Onsite, Shift Work Schedule (includes weekends, and possibly nights) Once shift is determined shifts will be on a stable schedule.
Must have: Manufacturing and PQA background
Responsibilities
- Provide on-going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations.
- Ensure that facilities, equipment, materials, organization, processes, and procedures comply with applicable regulations and Amgen requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and other controls.
- Drive closure/completion (including review and approve) of cGMP processes, procedures, documents and records, including but not limited to deviations, investigations, corrective action/preventative actions (CAPA)s.
- Ensure production and testing records/results are complete, accurate, and documented according to procedures, GDP and cGMP requirements.
- Oversee and provide guidance during on-the-floor analytical testing.
- Ensure that changes that could potentially impact product quality are assessed according to procedures.
- Ensure that deviations from established procedures are investigated and documented per procedures.
- Alert senior management of quality, compliance, supply and safety risks.
- Provide project management support, leading efforts to drive timely achievement of tasks and develop strategies for system implementation.
- Identification and implementation of continuous improvement opportunities within our processes and systems.
- Support and represent PQA during audits and inspections; may directly interact with regulatory agencies during on-site inspections.

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