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Spring Co-op/Drug Product Operations

GSK

Department Description

Are you looking for an impactful role that leverages your technical skills, organizational skills and ability to build exceptional relationships with trusted global partners to develop an increased number of transformative medicines for our patients? If so, this Drug Product Operations co-op role in a rapidly growing, empowered, innovative and agile Strategic External Development organization developing transformative medicines could be an ideal opportunity for you. The co-op may be completed at GSK's Upper Providence, PA or Waltham, MA site.


Job Description

As a co-op, you will contribute to internal and external development of the company's drug products. Responsibilities include:
  • Support and track clinical site inquiries.
  • Benchmarking of drug product package inserts (e.g. preparation and administration of IV products).
  • Support the drug product team on CMC (chemistry, manufacturing & controls) development teams to provide technical expertise and direction for drug product formulation development, early process development, scale-up, and technology transfer.
  • Review batch manufacturing data against protocols for accuracy and completeness.
  • Support material management using inventory management software.
  • Work with internal and external stakeholders to define and interpret development data results for CMC related activities in support of global clinical development, product registration and process qualification.


Minimum Qualifications

  • Pursuing a degree in Biological or Chemical Science, Engineering, Pharmaceutical Sciences, or similar technical disciplines.
  • Must be able to work full-time (35-40 hours/week) throughout the duration of the assignment.
  • Must have an active student status and/or within 12 months post-graduation from a BS or MS degree program. Post-doctoral candidates are not eligible.
  • Excellent communication skills, both oral and written.
  • Evidence of leadership and teamwork skills.
  • Desire for a career in the pharmaceutical industry.


Preferred Qualifications

  • Experience in biopharmaceutical/pharmaceutical industry or equivalent.
  • Experience with DoE software (e.g. JMP, Statistica).
  • Basic knowledge of the interrelationships between formulation, process development, and drug delivery. 


Eligibility Requirements

  • Must successfully pass a drug screen and background check prior to assignment target start date.
  • Must provide your own funding for relocation and commuting.
  • If your skillsets are a match for this role, you will be contacted by our recruitment team with next steps to complete our internal World of GSK Assessment.
  • Please note, you must receive a passing score to move forward in the interview process. Once your assessment is complete, a recruiter will review your results and be in touch with next steps.


Requisition Disclaimer

If you are hired for an on-site role, you will be required to provide Atrium with proof of COVID-19 Vaccination as a part of the on-boarding process on behalf of GSK. GSK has made the decision to require all US employees to be fully vaccinated against COVID-19, where allowed by state or local law and where vaccine supply is readily available. The only exceptions to this requirement are employees who are approved for an accommodation for religious, medical, or disability-related reasons.