Supervisor, Packaging Operations - Pharma

Supervisor, Packaging Operations - Pharma

Join to apply for the Supervisor, Packaging Operations - Pharma role at Gilead Sciences

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID‑19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.

Every member of Gilead’s team plays a critical role in the discovery and development of life‑changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.

We believe every employee deserves a great leader. People leaders are the cornerstone to the employee experience  a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations.

Act as a mentor to junior staff with some task management responsibility.
Personnel management of a team or shift.
May lead a special project team within the unit/function.
May serve as a team representative on cross‑functional projects in support of more senior colleagues in the function.
This is an advanced position requiring significant expertise/specialization in the area of work.
Works on complex issues where analysis requires an in‑depth assessment, considering many variables, and potential consequences.
Demonstrates proficiency in regulatory affairs and applies knowledge to processes.
Writes and/or implements changes to controlled documents (e.g., SOPs, Specifications, Methods, etc.) as needed.
Exercises judgment within well‑defined and established procedures and practices to determine appropriate action with minimal supervision.
Develops solutions to moderately complex problems and conducts final reviews prior to batch release approval by manager.
Supervises personnel including organizing and prioritizing daily tasks, performing training and writing performance reviews.
Plans/schedules packaging line equipment and staffing to meet production requirements.
Responsible for line output, performance and quality.
Demonstrates advanced technical knowledge.
Demonstrated success in leading projects and applying problem‑solving skills.
Demonstrates the ability to clearly and concisely present/explain process/product features, performance, and deviations to multiple internal audiences.
Demonstrates an ability and desire to supervise and support junior staff.
Demonstrates an ability to communicate effectively with peers in the organization.
Demonstrates the ability to think outside of the process and consider the impact decisions will have on other areas.
Provides hands‑on guidance to lower‑level Packaging Technicians.
Has daily contact with Compliance, Inventory Control and Maintenance to ensure equipment and materials are ready and available for use.
Investigates and reports variance or deviation from standard procedures to department management.
Conducts technicians’ performance evaluations and one‑on‑one meetings.
Assigns daily job responsibilities.
Expedites production scheduling through communication with QA/QC and Inventory Control personnel.
Participates in production processes, including cleaning and set‑up.
Complies with all established SOPs in performance of job; adheres consistently to GMPs.
Audit and investigation skills, report writing skills.
Proficient knowledge of Good Manufacturing Practices (GMPs).

• 6+ years of relevant experience and a BS or BA.
• 4+ years of relevant experience and a MS.
• Prior experience in a cGMP related industry is desirable, within Biopharmaceutical or Pharmaceutical industry preferred.

• Strong verbal, technical writing and interpersonal skills.
• Proficiency in Microsoft Office applications.
• Strong knowledge of the FDA and cGMP standards as well…