
This is Us:
You know us. You just didn’t know it. WACKER is a global chemical manufacturer that prides itself on “Creating Tomorrow’s Solutions”. WACKER materials are so versatile and adaptable, they have virtually unlimited applications just about anywhere imaginable, making WACKER an integral part of daily life. Whether it’s protecting buildings from the elements, a tube of toothpaste, a cell phone, airbags, or cosmetics, people from all over the world come into contact each day with our products and achievements. We are looking for capable, innovative, and enthusiastic achievers to join our team and grow with us. We are currently seeking a Senior Computer System Validation (CSV) Specialist at the site in San Diego, CA.
What you will do:
The Senior Computer System Validation (CSV) Specialist is an essential position in the CSV team. This position will be responsible of leading the implementation of lab instrument, manufacturing equipment and enterprise system that is used in Wacker Biotech San Diego site.
The position will entail building strong cross-functional relationships throughout the organization and translating requirements into CSV project. The role will also require supporting internal/external audits and other computer system lifecycle activities as required for the CSV program, as well as be responsible to develop and execute CSV lifecycle related deliverables with minimum supervision.This role will be leading the periodic review of validation computerized system and generate a periodic review report. This role will be supporting system owner on other computer system compliance activities like audit trail review, security review, and annual backup restore testing.
The Senior CSV Specialist will support global computer system validation project from the Global Bio-digital Solution team and provide Veeva QMS/EDMS/Training Vaults administration as required.
- Leading implementation of computerized system and perform CSV validation activities per WBU procedure.
- Perform CSV lifecycle activities including periodic review, audit trail review, security review, backup restore testing and other activities defined per WBU SOP.
- Support global computer system implementation and validation.
- Provide CSV support in deviation, CAPA, Change Control, and computer system vendor evaluation.
- Support regulatory filings and inspection as CSV SME.
- Support CSV remediation activities from external and internal audit.
What we need from you:
- Bachelor’s degree in science with 6+ years or MS/PhD with 4+ years of GMP/Relevant Industry Experience. (Chemistry, biochemistry, or related discipline preferred).
- Must have 4+ years of experience in pharmaceutical (FDA regulated industry) computer system validation.
- Ability to travel less than 10%.
- Proficient understanding of GMP, GAMP, Annex 11, 21CFR
- Lead and implement CSV project with minimum supervision.
- Must have strong hands-on, end-to-end validation experience and application of project controls / management - including familiarity with all project lifecycle phases from requirements gathering through delivery, issues / risk management, change management, release management and retirement management.
- Experience with wide range of CSV experience including Manufacturing, Lab and Enterprise CSV experience.
- Implementing change initiatives and leading change.
- Statistical analysis
- Excellent analytical interpretation skills
- Risk-based application of validation principles
- Committed to delivering high quality results, overcoming challenges, focusing on what matters
- Strong problem solving and decision-making skills
- Good organizational skills and attention to detail.
- Requires good written, verbal, and interpersonal communication skills and the ability to effectively interact with all levels.
- Ability to handle multiple assignments and changing priorities.
- Positive, proactive approach to drive assignments/tasks to completion.
- Proficiency with Microsoft Word, Excel, PowerPoint
- Ability or capable of lifting up to fifty (50) lbs.
The anticipated salary range for candidates who will work in San Diego is $100,000 – 130,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc . Wacker is a multi-state employer, and this salary range may not reflect positions that work in other states.
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Compensation and Incentive plans
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Medical, Dental, and Vision Insurance effective day 1
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Paid Time Off in addition to personal days and holidays
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Paid parental leave
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Wellbeing fund
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Flexible hybrid work arrangements
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401(k) with company match
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Education Assistance Program
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Career development and advancement opportunities
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Support for Community Involvement
Reference Code: 29283
Nearest Major Market: San Diego