validation manager

<div>Site Name: Egypt - Cairo 
Posted Date: Mar 18 2026 
We manufacture and supply reliable, high-quality medicines and vaccines to meet patients&rsquo; needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it&rsquo;s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.
Validation Section Head
You will lead a team that plans, executes and maintains validation activities at our Egypt site. You will work with Quality, Production, Technical Services and Regulatory teams to ensure processes, equipment and systems meet compliance and quality standards. We value people who are practical, curious and focused on safety and continuous improvement. This role offers clear growth, visible impact on product quality and the chance to apply science, technology and talent to get ahead of disease together.
Responsibilities:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:<ul><li>Lead the validation section and own the Site Validation Master Plan and related priorities.</li><li>Design, review and approve process, cleaning, bulk holding time, air and water system validation protocols and reports.</li></ul>
-Coordinate different thermal mapping activities (initial qualification and thermal mapping review) -Prepare required validation life cycle documents (not limited to: DR, RTM, CDA, IQ, OQ, PQ, Validation reviews, PQ reports and VSRs) for different activities for process equipement and utilities upgrade in accordance to validation lifecycle and CSV requirements.<ul><li>Handling calibration program for Lab instruments.-Maintain validation lifecycle records and keep systems inspection ready through periodic reviews and self-inspections.</li><li>Support investigations, change controls and CAPAs linked to validation activities and lead root cause analysis with cross-functional teams.</li><li>Coach and develop team members, share best practice, and drive continuous improvement in validation methods and documentation.</li></ul>
Why you?
This role is on-site in Egypt. Hybrid or remote working arrangements are not available for this role. 
Basic Qualification:
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:<ul><li>Bachelor&rsquo;s degree in pharmaceutical science, pharmacy, engineering, chemistry or a related scientific discipline.</li><li>Minimum 4 years of relevant experience in pharmaceutical validation, quality or production in a regulated environment.</li><li>Hands-on experience with process validation, cleaning validation, and bulk holding time studies.</li><li>Hands-on experience with Equipment,systems and CSV qualification.</li><li>Hands-on experience with Lab Instrument calibration.</li><li>Solid knowledge of good manufacturing practice and data integrity expectations.</li><li>Strong written and spoken English and effective communication skills.</li></ul>
Preferred Qualification:<div>
If you have the following characteristics, it would be a plus: 
<ul><li>Experience leading teams or supervising validation activities.</li><li>Knowledge of validation lifecycle management tools and quality management systems.</li><li>Familiarity with computer system validation and data integrity controls for IT systems.</li><li>Experience with statistical sampling methods and tools for validation decisions.</li><li>Experience supporting regulatory inspections and technical risk assessments.</li><li>Previous exposure to sterile manufacturing and complex dosage forms.</li></ul></div>
Working arrangement
This role is on-site in Egypt. Hybrid or remote working arrangements are not available for this role.
What we offer in this role
You will have clear ownership of critical validation activities that protect product quality and patient safety. You will work with supportive colleagues across functions and gain practical leadership experience. You will influence processes, build capability in your team and grow your technical and management skills
Apply now
If this role interests you, we encourage you to apply. We welcome people with different backgrounds and experiences. Join us and help bring science, technology and talent together to get ahead of disease.
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Contact information: 
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div>

Validation Section Head

Zifo

<div>Responsible for validation strategy and planning, executing and qualification of computer systems and/or infrastructure components in accordance with applicable policies procedures and regulatory requirements 
Requirements 
<ul><li>
Define validation Strategy for computerized systems and platforms utilized in GxP Space</li><li>
Create Validation deliverables such as Validation Plan, Test Protocols, Traceability matrix and execution of protocols</li><li>
Participate in user review meetings, discussions with Quality Assurance and Compliance groups</li><li>
Participate/conduct Risk Assessments</li><li>
Develop and maintain policies and procedures</li><li>
Effectively communicate the validation activities and deliverables to the project team, customer stake holders and global team within Zifo</li><li>
Act as a liaison between Zifo remote teams and customers in US &amp; Canada</li><li>
Participate in internal initiatives around Computer Systems Validation</li></ul>
Qualifications<ul><li>
Bachelor or Master&rsquo;s degree in Lifesciences or Computer Sciences</li><li>
5+ years&rsquo; experience with Computer Systems Validation is required for this role</li><li>
Strong knowledge of GxP Requirements, GCP regulations, 21 CFR part 11 requirements</li><li>
Must have experience with validation of IT infrastructure systems including R, SAS etc.</li><li>
Experience with GxP systems validation like ELN, LIMS, QMS etc.</li><li>
Experience with Veeva Vault Systems</li></ul> 

Benefits 
CURIOSITY DRIVEN, SCIENCE FOCUSED, EMPLOYEE BUILT. Our culture is unlike any other, one where we debate, challenge ourselves, and interact with all alike. We are a curious bunch, characterized by our passion to learn and spirit of teamwork. Zifo is a global R&amp;D solutions provider focused on the industries of Pharma, Biotech, Manufacturing QC, Medical Devices, specialty chemicals and other research-based organizations. Our team&rsquo;s knowledge of science and expertise in technology help Zifo better serve our customers around the globe, including 18 of the Top 20 Biopharma companies.
We look for Science &ndash; Biotechnology, Pharmaceutical Technology, Biomedical Engineering, Microbiology etc. We possess scientific and technical knowledge and bear professional and personal goals. While we have a &ldquo;no doors&rdquo; policy to promote free access within, we do have a tough door to walk in. We search with a two-point agenda &ndash; technical competency and cultural adaptability.
We offer a competitive compensation package including accrued vacation, medical, dental, vision, 401k with company matching, life insurance, and flexible spending accounts.
If you share these sentiments and are prepared for the atypical, then Zifo is your calling!
Zifo is an equal opportunity employer, and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.</div>

CSV Validation Engineer

Spadtek Solutions LLC

Job Description:We are seeking a highly experienced CQV Lead to drive Commissioning, Qualification, and Validation activities for large-scale capital projects within a GMP-regulated pharmaceutical/biotech environment. The ideal candidate will be responsible for leading CQV strategy, execution, and ensuring compliance with regulatory standards.Key Responsibilities:<ul><li>Lead CQV strategy and execution for capital projects (greenfield/brownfield)</li><li>Develop and review validation lifecycle documents (URS, DQ, FAT, SAT, IQ, OQ, PQ)</li><li>Oversee commissioning and qualification of process equipment, clean utilities, and facilities</li><li>Ensure compliance with cGMP, FDA, and global regulatory requirements</li><li>Collaborate with Engineering, QA, Manufacturing, and Project teams</li><li>Manage CQV timelines, deliverables, and resources</li><li>Support regulatory inspections and audits (FDA, EMA, etc.)</li><li>Identify risks and implement mitigation strategies</li><li>Mentor and guide junior CQV engineers</li></ul>Required Qualifications:<ul><li>15+ years of CQV experience in Pharma/Biotech industry</li><li>Strong experience with large-scale capital projects</li><li>Hands-on validation experience (equipment, utilities, facilities)</li><li>In-depth knowledge of cGMP, FDA regulations, and validation lifecycle</li><li>Proven leadership and team management skills</li><li>Strong communication and documentation skills</li></ul>Preferred Qualifications:<ul><li>Bachelor&rsquo;s/Master&rsquo;s degree in Engineering (Chemical, Mechanical, or related)</li><li>Experience in cleanroom validation, aseptic processing, or biologics manufacturing</li><li>Familiarity with HVAC, WFI, CIP/SIP systems and process automation</li></ul>Pay: $45.00 - $50.00 per hourWork Location: In person

CQV Lead (Pharma/Biotech)

Banc of California

<div>BANC OF CALIFORNIA AND YOUR CAREER

Banc of California, Inc. (NYSE: BANC) is a bank holding company with over $34 billion in assets and the parent company of Banc of California. Banc of California is one of the nation&rsquo;s premier relationship-based business banks, providing banking and treasury management services to small, middle market, and venture backed businesses. As the largest independent bank headquartered in California, the bank offers a broad range of loan and deposit products and services through a network of full-service branches and regional offices, as well as through digital and nationwide capabilities. The bank also provides full-service payment processing solutions to its clients and serves the Community Association Management industry nationwide through its technology forward platform, SmartStreet&trade;. Banc of California is committed to supporting its local communities through the Banc of California Charitable Foundation and by partnering with organizations that promote financial literacy, job training, small business support, affordable housing, and more.

At Banc of California, our success is powered by our people and a shared commitment to delivering meaningful results. We foster an environment where entrepreneurial thinking is encouraged, and accountability and operational excellence are expected. Our team members are empowered to take ownership, make informed decisions, and make a meaningful impact as the bank continues to grow and evolve. We are dedicated to supporting your growth and wellbeing through comprehensive benefits, robust development opportunities, and inclusive programs that enable you to perform at your best. Together we win!

THE OPPORTUNITY

The Vice President, Model Validation is responsible for assisting the Bank&rsquo;s Model Risk Management with its framework and standards, model inventory, model risk assessment, model validation and model governance. Performs all duties in accordance with the Company&rsquo;s policies and procedures, all U.S. state and federal laws and regulations, wherein the Company operates 


HOW YOU&rsquo;LL MAKE A DIFFERENCE
<ul>
<li>Conduct model validations on the Bank&rsquo;s models, both in-house and vendor models, based on regulatory guidelines, the Bank&rsquo;s model risk management policy and procedure, and the industry&rsquo;s leading practices.</li>
<li>Evaluate model assumptions and weaknesses, data relevancy and completeness, conceptual soundness, modeling methodology, outcome analysis, etc.</li>
<li>Prepare a model validation report that meets the Model Risk Management&rsquo;s expectations, based on the evaluation of the model, including backtesting, sensitivity testing, benchmarking, etc. and include a conclusion based on the review.</li>
<li>Assist in model validation findings monitoring, reporting, and evaluating the corrective actions.</li>
<li>Conduct model annual reviews including process verification, performance monitoring, degree of changes, etc. and document the findings and comments in the annual review report.</li>
<li>Support senior managers to communicate findings and recommendations from model validation report to model owners and model users.</li>
<li>Work closely with model owners and model users to understand the model use and business applications.</li>
<li>Review on-going model monitoring report, identify potential model risks; document the findings</li>
<li>Treat people with respect; keep commitments; inspire the trust of others; work ethically and with integrity; uphold organizational values; accept responsibility for own actions.</li>
<li>Demonstrates knowledge of and adherence to EEO policy; shows respect and sensitivity for cultural differences; educates others on the value of diversity; promotes working environment free of harassment of any type; builds a diverse workforce and supports affirmative action.</li>
<li>Follows policies and procedures; completes tasks correctly and on time; supports the company&rsquo;s goals and values.</li>
<li>Performs the position safely, without endangering the health or safety to themselves or others and will be expected to report potentially unsafe conditions. The employee shall comply with occupational safety and health standards and all rules, regulations and orders issued pursuant to the OSHA Act of 1970, which are applicable to one&rsquo;s own actions and conduct.</li>
<li>Performs other duties and projects as assigned.</li></ul> 


WHAT YOU&rsquo;LL BRING
<ul>
<li>6+ years&rsquo; experience in model validation or model development in the banking industry or consulting.</li>
<li>Master&rsquo;s in Economics, Finance, Mathematics and/or other related quantitative fields.</li>
<li>Familiarity with model documentation requirements that meets regulatory expectations.</li>
<li>Strong written and verbal communication skills.</li>
<li>Familiarity with dealing with large data set.</li>
<li>Experience with model validation..</li>
<li>Proficiency in statistical programming skills such as in Python / R.</li>
<li>Strong organizational, written and verbal communication skills.</li>
<li>Ability to work independently and collaboratively.</li>
<li>Ability to interface effectively and professionally with senior level management.</li>
<li>Ability to multi-task several projects at once.</li>
<li>Excellent attention to detail and accuracy</li>
<li>Excellent organizational and time management skills.</li>
<li>Proven ability to use Microsoft Office Suite (Outlook, Excel, MS Word, and PowerPoint).</li>
<li>Creative and strategic thinker capable of analyzing information/processes to determine overall trends and make appropriate conclusions.</li>
<li>Review and be knowledgeable of departmental and human resource&rsquo;s policies &amp; procedures</li>
</ul>
Preferred:
<ul>
<li>Experience with BSA/OFAC, Payment, or Merchant Acquiring/Card Issuing model validation.</li>
<li>Familiarity with AI/ML models</li></ul> 


HOW WE&rsquo;LL SUPPORT YOU
<ul>
<li>Financial Security: You will be eligible to participate in the company&rsquo;s 401k plan which includes a company match and immediate vesting.</li>
<li>Health &amp; Well-Being: We offer comprehensive insurance options including medical, dental, vision, AD&amp;D, supplemental life, long-term disability, pre-tax Health Savings Account with employer contributions, and pre-tax Flexible Spending Account (FSA).</li>
<li>Building &amp; Supporting Your Family: Banc of California partners with providers that offer adoption, surrogacy, and fertility assistance as well as paid parental leave and family support solutions including care options for your family.</li>
<li>Paid Time Away: Eligible team members receive paid vacation days, holidays, and volunteer time off.</li>
<li>Career Growth Opportunities: To support career growth of our team members, we offer tuition reimbursement, an annual mentorship program, leadership development resources, access to LinkedIn Learning, and more.</li></ul> 


SALARY RANGE

The base salary ultimately offered is determined through a review of education, industry experience, training, knowledge, skills, abilities of the applicant in alignment with market data and other factors.

Banc of California is an equal opportunity employer committed to creating a diverse workforce. All qualified applicants will receive consideration for employment without regard to age (40 and over), ancestry, color, religious creed (including religious dress and grooming practices), denial of Family and Medical Care Leave, disability (mental and physical) including HIV and AIDS, marital status, medical condition (cancer and genetic characteristics), genetic information, military and veteran status, national origin (including language use restrictions), race, sex (which includes pregnancy, childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), gender, gender identity, gender expression, and sexual orientation. If you require reasonable accommodation as part of the application process, please contact Talent Acquisition.</div>

VP, Model Validation

Bristol Myers Squibb

<div>Working with Us 
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. 
 
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . 
 
The Associate Director, Cell Therapy Network CQV, is responsible for the network strategy for equipment/facility/utility Commissioning, Qualification, and Validation. The scope encompasses the internal CT manufacturing sites and engagement with external CMOs via Virtual Plant Teams. This role will partner cross-functionally with site CQV leads, site equipment owners, Cell Therapy network Digital Plant leaders, the BMS QMS Qualification Global Process Owner, and CTTO Global Equipment Owners. 
 
Key Responsibilities:<ul><li>
Establish strategy and deliver optimized and harmonized CQV approaches across the Cell Therapy network.</li><li>
Work collaboratively with Cell Therapy network Digital Plant and BMS enterprise qualification L2 to synthesize guidance in standards for qualification of equipment with internal computer systems.</li><li>
Oversight of Cell Therapy equipment validation execution across network, ensuring lifecycle management of the standardized approach.</li><li>
Responsible for ensuring all regulatory and GxP compliance items related to Validation are satisfied, maintaining all sites in an inspection-ready status.</li></ul>
Qualifications &amp; Experience:<ul><li>
B.S., M.S., or Ph.D. in Mechanical Engineering, Chemical Engineering, or related scientific/engineering discipline with: 15+ years w/ B.S. or 12 years w/ M.S. or 8 years w/ Ph.D. of experience in biologics or cell therapy GMP manufacturing support.</li><li>
Strong understanding of CMC regulatory requirements, DS &amp; DP manufacturing, and analytical testing.</li><li>
Excellent strategic thinking, problem-solving, decision-making, and communication skills.</li><li>
Strong knowledge of ICH guidelines, control strategies, and validation lifecycle frameworks.</li><li>
Ability to effectively utilize project management and Lean Six Sigma tools is a plus.</li><li>
Excellent interpersonal, collaborative, team building, and communication skills.</li></ul>
#LI-Hybrid 
 
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
 
 
Compensation Overview: 
 
Devens - MA - US: $175,750 - $212,973 
Madison - Giralda - NJ - US: $164,260 - $199,048 
Princeton - NJ - US: $164,260 - $199,048
 
Seattle - WA: $180,680 - $218,947 
 
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
 
 
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
 
 
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
<ul><li>Health Coverage: Medical, pharmacy, dental, and vision care.</li><li>
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
</li><li>Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
</li></ul>Work-life benefits include:
 
 
Paid Time Off
<ul><li>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
</li><li>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
</li></ul>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
 
 
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. 
 
<ul><li>Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
</li></ul> 
Uniquely Interesting Work, Life-changing Careers 
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. 
 
On-site Protocol 
 
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
 
 
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
 
 
Supporting People with Disabilities 
 
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
 
 
Candidate Rights 
 
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
 
 
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
 
 
Data Protection 
 
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection . 
 
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. 
 
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
 
 
R1599924 : Associate Director, Cell Therapy Network CQV</div>

Associate Director, Cell Therapy Network CQV

Search 10000+ Validation manager jobs near you this March. New roles added regularly across leading industries. Apply today.

10000 validation manager jobs Near Me

Validation Section Head

CSV Validation Engineer

CQV Lead (Pharma/Biotech)

VP, Model Validation

Associate Director, Cell Therapy Network CQV

Associate Director, Cell Therapy Network CQV

Associate Director, Cell Therapy Network CQV