Manufacturing Tech IV
- Employer
- Gilead Sciences, Inc.
- Location
- Foster City
- Salary
- See job description.
- Closing date
- Aug 19, 2021
View more
- Discipline
- Other, Manufacturing/QA/QC
- Position Type
- Full Time
- Job Type
- Technician
- Organization Type
- All Industry, Pharma
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Manufacturing Tech IV
United States - California - La Verne
Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gileads therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.
Making an impact on a global scale
Inclusion is one of the companys five core values. Thats because we know that we are stronger and more innovative at Gilead when we are informed by a diverse set of backgrounds, experiences and points of view. Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide.
When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible
Manufacturing Tech IV
This is a semi-experienced position requiring working or specialized knowledge of manufacturing systems, methods and procedures. Assignments range from routine to basic where analysis of situation or data requires a review of moderately complex factors., Candidate will work on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Additionally, they may be assigned as a lead or point on a single project while demonstrates significant capability to troubleshoot unassisted
Job Responsibilities
- Works on basic to routine assignments following established Standard Operating Procedures (SOPs), Master Batch Records and current Good Manufacturing Practices (cGMPs).
- Reports to Team Lead on a regular basis on line performance and reports any issues that need to be resolved.
- Performs more complex troubleshooting unassisted
- Works on more complex manufacturing processes and assignments
- Works in conjunction with other manufacturing technicians under the guidance of a Team Leader
- Assists in manufacturing product, moves materials and prepared product to appropriate locations in accordance with SOPs.
- Sets up, operates, and troubleshoots equipment in classed clean room environments.
- At the end of shifts, secures all equipment and machinery, and completes all required paperwork.
- Cleans (manually and CIP) and assembles equipment for production.
- Interacts with scientists, engineers, and production staff.
- Records product and order information on specified forms and records.
- Examines and inspects containers, materials, and products to ensure that specifications are met.
- May train junior staff in assigned area, and ensure that work is performed in accordance with quality standards and SOPs.
Knowledge and Skills
- Knowledge of current Good Manufacturing Practices (GMPs).
- Demonstrates good verbal, written, and interpersonal communication skills.
- Receives general instructions on routine work, and detailed instructions on new assignments.
- Follows written Standard Operating Procedures (SOPs) and Master Batch Records and must be able to take variant action only with approval of department management.
- Independent action and initiative in resolving issues.
- Demonstrates strong safety orientation, with strict adherence to established safety practices and standards.
- Takes independent action and initiative in resolving issues.
Basic Qualifications
- 5+ years of relevant experience, HS Diploma
- Prior experience in a cGMP related industry is required.
For jobs in the United States:
As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job 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 careers@gilead.com for assistance.
For more information about equal employment opportunity protections, please view the EEO is the Law' 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 log onto your Internal Career Site to apply for this job.
To apply, visit https://gilead.wd1.myworkdayjobs.com/en-US/gileadcareers/job/United-States---California---La-Verne/Manufacturing-Tech-IV_R0021232
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