Senior CQV Engineer & Lead — Pharma Validation

Energy Jobline ZR; Boston (MA); Presencial; USD 70 000 - 110 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Life, Short-Term & Long-Term Insurance

Medical, Dental & Vision Insurance

401(k) with Employer Match

Paid Time Off & Holidays

Tuition Reimbursement

Employee Referral Program

Parental Leave & Bereavement

Resumo da oferta

Verista is seeking a Senior CQV Engineer to join our Boston-area team. You will lead CQV activities for pharmaceutical manufacturing, design validation plans, assess risk, and maintain detailed records to support compliance audits.

Strong communication and GMP experience are essential as you mentor colleagues and collaborate with clients onsite. The role requires 4–6 years of experience, on-site work in the Boston metro area and travel up to 50%.

Qualificações

• Bachelor's Degree or equivalent required.
• 4–6 years of demonstrated role relevant experience.
• Demonstrated experience in leading CQV activities specific to pharmaceutical manufacturing requirements.
• GMP regulated environment experience.
• Ability to work onsite in the Boston metropolitan area.
• Willingness to travel 10–50%.

Responsabilidades

• Designing validation plans and documenting impact/risk assessments.
• Maintaining qualification and validation records for audits.
• Designing and executing studies for parameter definition and verification prior to validation.
• Authoring and executing commissioning, qualification, and validation documentation.
• Running test scripts and documenting results; adhering to project schedules.
• Mentoring and guiding less experienced team members.

Conhecimentos

CQV leadership

Communication

Team collaboration

Problem solving

Time management

Attention to detail

GMP & GDP

On-site work

Formação académica

Bachelor's Degree or equivalent

Ferramentas

Microsoft Office

Descrição da oferta de emprego

Verista is seeking a Senior CQV Engineer to join our Boston-area team. You will lead CQV activities for pharmaceutical manufacturing, design validation plans, assess risk, and maintain detailed records to support compliance audits.

Strong communication and GMP experience are essential as you mentor colleagues and collaborate with clients onsite. The role requires 4–6 years of experience, on-site work in the Boston metro area and travel up to 50%.