drjobs Manufacturing Team Lead

Manufacturing Team Lead

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1 Vacancy
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Job Location drjobs

La Verne, CA - USA

Monthly Salary drjobs

$ 99705 - 129030

Vacancy

1 Vacancy

Job Description

At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID19 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 worlds biggest health challenges and our mission requires collaboration determination and a relentless drive to make a difference.

Every member of Gileads team plays a critical role in the discovery and development of lifechanging scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions and were 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 at Gilead and Kite. As 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. Join Gilead and help create possible together.

Job Description

Manufacturing Team Lead

Role and Responsibilities:

Manages a team or shift of personnel and serves as a mentor to junior staff.

Has an ability to communicate clearly and effectively with peers within the organization.

Leads special team projects within the manufacturing unit/function.

Serves as a representative on crossfunctional projects to support more senior colleagues in the function.

Exercises diplomacy and critical thinking skills while troubleshooting issues with internal and external groups.

Clearly and concisely explains process/product features performance and deviations to multiple audiences.

Manages the storage replenishment usage and discarding of hazardous and volatile chemicals.

Performs a daily thorough check of the equipment and clean room areas and follows through with service requests to for maintenance/automation/facilities teams to correct identified issues.

Essential Duties and Job Functions:

Attends mandatory company training and ensures he/she is trained on production processes.

Provides hands on guidance to Manufacturing technicians.

Conducts technicians performance evaluations one on one meetings and quarterly check ins.

Expedites production scheduling through communication with QA/QC and Inventory Control personnel.

Delegates and oversees corrective maintenance work orders for clean room equipment and rooms.

Establishes and maintains 6S housekeeping standards for manufacturing owned areas.

Maintains an accurate inventory of product components within L10 storage locations.

Supervises personnel including organizing and prioritizing daily tasks performing/scheduling training writing performance reviews.

Works on complex issues where analysis requires an indepth assessment considering many variables and potential consequences.

Uses advanced statistical techniques to complete projects.

Uses more complex research techniques and methodologies like Six Sigma and Kaizen to improve process/product quality.

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 of logbooks and production records prior to batch release.

Knowledge Experience and Skills:

Demonstrates strong knowledge of Good Manufacturing Practices (GMPs) and working knowledge of regulatory filing requirements and guidance documents (i.e. SUPAC PACPAC).

Is able to provide solutions to moderately complex to semiroutine problems.

Demonstrates excellent verbal written and interpersonal communication skills.

Demonstrates strong computer organizational and project management skills.

Demonstrates ability to recognize deviation from accepted practice.

Demonstrates ability to apply knowledge of current Good Manufacturing Practices (cGMPs) daily.

Demonstrates ability to successfully supervise and support junior staff.

Basic Qualifications:

At least 6 years of relevant experience and a BS or BA.

At least 4 years of relevant experience and a MS.

Prior experience in a cGMP related industry is required within Biopharmaceutical or Pharmaceutical industry preferred.

At least 2 years of prior people management preferred.

Flexibility to work 12hour shifts that cover 24/7 production schedules (including all major US Holidays)


The salary range for this position is: $99705.00 $129030.00. Gilead considers a variety of factors when determining base compensation including experience qualifications and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus discretionary stockbased longterm incentives (eligibility may vary based on role) paid time off and a benefits package. Benefits include companysponsored medical dental vision and life insurance plans*.

For additional benefits information visit:

Eligible employees may participate in benefit plans subject to the terms and conditions of the applicable plans.


For jobs in the United States:

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment and is dedicated to fostering an inclusive work environment comprised of diverse perspectives backgrounds and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race color religion national origin sex age sexual orientation physical or mental disabilitygenetic information or characteristic gender identity and expression veteran status or other nonjob related characteristics or other prohibited grounds specified in applicable federal state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973 the Vietnam Era Veterans Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990 applicants who require accommodation in the job application process may contact for assistance.


For more information about equal employment opportunity protections please view the
Know Your Rights poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

PAY TRANSPARENCY NONDISCRIMINATION PROVISION

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.


For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Employment Type

Full-Time

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