Planet Pharma
Planet Pharma

1 Planet Pharma Validation Engineer Jobs Hiring Near You

Identify process discrepancies and collaborate with LCM and Process Engineering for improvement. * Support maintaining the validated state by providing SME support on Validation plans, verification ...

Planet Pharma Jobs Information

What is it like to work at Planet Pharma?

Planet Pharma appears to be a collaborative and innovative company that prioritizes teamwork and open communication in its work environment. The company's mission is focused on providing high-quality services and solutions to the pharmaceutical industry, with a team structure that includes professionals from various backgrounds and expertise. Working at Planet Pharma may appeal to candidates who are interested in contributing to the development of cutting-edge solutions and technologies in the pharmaceutical sector.

What makes Planet Pharma an attractive place to work?

Planet Pharma is a leading provider of clinical research services, offering a unique blend of expertise and technology to support the development of innovative pharmaceutical products. The company's workplace is characterized by a culture of innovation, collaboration, and continuous learning, with opportunities for employees to work on complex projects and contribute to the advancement of medical research. By joining Planet Pharma, professionals can expect to be part of a dynamic and growing organization that offers opportunities for career growth, professional development, and making a meaningful impact in the pharmaceutical industry.

What other companies are hiring for Validation Engineer jobs?

Manufacturing Specialist

Planet Pharma

Hayward, CA • On-site

$28 - $31/hr

Other

Posted 24 days ago


Job description

629651 Manufacturing Specialist 1

Hayward, CA

6 month contract


Fast learner

Able to work independently

Familiar with Microsoft Office applications

Able to use hand tools/torque tools, lift 15 lbs

OT available on weekends.


Job Summary: Responsible for technical and process support to the manufacturing team in order to effectively achieve production plans while maintaining quality and compliance to Quality Systems


Tasks and responsibilities:

  • Analyze production data to determine trends and define actions to improve efficiency, product quality and cost.
  • Identify process discrepancies and collaborate with LCM and Process Engineering for improvement.
  • Support maintaining the validated state by providing SME support on Validation plans, verification and validation protocols and executing on released protocols.
  • Act as SME during development and change management on MES and eDHR process and systems by collaborating with GIS, Process Engineering and Quality.
  • Support development and in some cases create or modify Quality Documents such as; work instructions, procedures, pFMEA’s validation test reports, batch record templates and test methods.
  • Proactively participate on continuous improvement teams and projects using techniques from Operational Excellence and Lean Six Sigma methodologies.
  • Participate in manufacturing internal audit program and assist with corrective actions and audit responses.
  • Test next generation DNA sequencing instrumentation using released procedures and processes.
  • Troubleshoot and process non-conformances of products while collaborating with Manufacturing, Quality and Life Cycle Management.
  • Establish and maintain reports of instrument failures and defects.
  • Other duties as needed.


All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities.


Required educational background:

  • High school diploma, GED.
  • Some relevant college level STEM courses or training are a plus.


Preferred educational background:

  • Bachelors (BA/BS) in Engineering, Chemistry, Biology, Physics.


Preferred experiential background:

  • Typically requires no previous technical experience.
  • Normally receives detailed instructions on all work.
  • Strong organizational skills, attention to detail and accuracy, and the ability to work independently in a team environment are essential.
  • Ability to collaborate on multifunctional teams and manage ambiguity.
  • Strong interpersonal, verbal and written communication skills.
  • Excellent troubleshooting skills required.
  • Proficiency with Microsoft Office Tools (Excel, Word, and PowerPoint)
  • Experience with SOPs, DHRs, ECOs, GLP, GMP and SAP ERP systems is a plus.
  • Hands on experience with clinical/diagnostic instrumentation including DNA sequencing or equivalent is highly desirable.


***Pay rate is commensurate with experience, target pay rate range is $28-31/hr