Associate I, Technical Development Operations
Planet Pharma
Location: South San Francisco, CA (100% On-site)
Position Type: 6-Month Contract (May extend or convert to permanent)
Schedule: M-F, 8:00 AM – 5:00 PM or 9:00 AM – 6:00 PM (Occasional weekend work, approx. one day/month)
Compensation: $40.54/hour W2
Perks: Free on-site parking!
About the Role
We are seeking a motivated, collaborative, and hands-on Associate to join our Technical Development Department within the Cell and Gene Therapy Research Division. This is a dynamic, lab-centric role (75% lab, 25% office) supporting both upstream and downstream process development activities , as well as operations in our pilot plant for gene therapy programs.
This is a fantastic entry-to-early career opportunity to gain hands-on experience with cutting-edge AAV (Adeno-Associated Virus) production and process development. The ideal candidate is someone with a strong desire to learn, a positive attitude, and a flexible mindset.
Top Skills & Experience We Are Looking For
- Experience Level: 0–3 years of bioprocess experience. Recent graduates with strong applicable educational backgrounds/internships and the right attitude are highly encouraged to apply!
- Education: BS in Life Sciences, Bioengineering, or a related discipline. (Please note: Master’s degrees will be considered based on motivation; PhD candidates are overqualified for this specific role).
- The Right Fit: Candidates with 5+ years of experience will not be a fit for this junior-level team structure. We care deeply about your mindset, coachability, and eagerness to dive into lab work.
Essential Job Responsibilities
- 75% Lab Operations: Set up, monitor, and take down experiments and equipment for both upstream and downstream processes.
- Upstream Duties: Execute experiments for cell culture and transfections in shake flasks and bioreactors (primarily Sartorius and Wave systems); maintain seed train cell cultures (vial thaws through expansions); perform cell culture harvest operations.
- Downstream Duties: Support purification unit operations including column packing, filtration, chromatography, and Tangential Flow Filtration (TFF).
- Documentation & Digital Records: Maintain meticulous digital records of all research production activities using in-house systems and shared digital document repositories; assist with document preparation and revisions.
- Safety & Collaboration: Follow all laboratory safety procedures, participate in safety meetings, and maintain a highly collaborative, positive attitude in a team-focused environment.
Qualifications
Required:
- BS in Life Sciences, Engineering, or equivalent experience.
- 0–2+ years of experience working in a pharmaceutical/biologics lab or manufacturing environment (Industry internships count!).
- Foundational understanding of upstream and/or downstream process theory (Cell Culture, Harvest, TFF, Column Chromatography).
- Strong communication skills and the ability to work effectively both independently and as part of a team.
- Proficiency with MS Office (Word, Excel, PowerPoint) and strong digital record-keeping skills.
- Flexibility to work outside of normal business hours/overtime as required (occasional weekend work, approx. once a month).
Preferred (Nice to Have):
- Direct experience with AAV or gene therapy processes.
- Experience with single-use/disposable manufacturing technologies (e.g., sterile bags, tubing welders).
- Ability to multi-task and thrive in a fast-paced, dynamic environment with changing priorities.
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