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Engineering Projects Senior Manager

Amgen

Engineering Projects Senior Manager

Amgen

India - Hyderabad

·

On-site

·

Full-time

·

1w ago

Benefits & Perks

Healthcare

401(k)

Learning Budget

Flexible Hours

Healthcare

401k

Learning

Flexible Hours

Required Skills

Commissioning and Qualification

Validation

GMP Compliance

Leadership

Project Management

Team Management

Technical Writing

Career Category

Project Management

Job Description Commissioning & Qualification (C&Q) Lead (Level 6) – Manager, C & Q Center of Excellence (CoE)Summary:The C&Q CoE Lead provides leadership and strategic direction for the Commissioning and Qualification (C&Q) activities within the broader manufacturing operations network. This role manages a small, high-performing team responsible for delivering C&Q documentation, test protocols, and execution summary reports and other C&Q lifecycle documents to ensure facility, utility, and equipment systems are fit for intended use and compliant with internal standards and regulatory expectations. The C&Q Program Lead drives standardization, efficiency, and continuous improvement in C&Q processes across projects and manufacturing functions.Key Responsibilities:Leadership & Team Management

  • Manage a team of C&Q engineers and specialists responsible for authoring, reviewing, and commissioning and qualification lifecycle documentation.

  • Set clear expectations, provide mentorship, and foster a culture of accountability, technical excellence, and collaboration.

  • Coordinate workload and resource allocation across multiple project workstreams to ensure timely delivery of C&Q milestones.

  • Support career development, training, and performance evaluations for direct reports.Program Oversight & Delivery

  • Serve as the primary C&Q representative to the Capital project leadership team, ensuring alignment of C&Q strategy, and prioritization with project goals, quality standards, and business needs.

  • Lead development and execution of the overall C&Q plan, including scope definition, risk assessment, protocol strategy, and system prioritization.

  • Oversee generation, review, and approval of C&Q documents such as User Requirements Specifications (URS), commissioning plans, qualification protocols (IQ/OQ/PQ), and summary reports.

  • Manage C&Q schedule, budget, and resource forecasting; identify risks and implement mitigation plans proactively.

  • Ensure adherence to applicable global standards, Good Manufacturing Practice (GMP) regulations, and data integrity requirements.Process Standardization & Continuous Improvement

  • Champion the implementation and maintenance of standardized C&Q practices, templates, and procedures across sites and projects.

  • Drive process improvements to enhance efficiency, consistency, and compliance in C&Q execution.

  • Collaborate with cross-functional partners (Engineering, Validation, Quality, Operations, and Global Facilities Delivery) to align on best practices and lessons learned.

  • Contribute to global C&Q governance initiatives and knowledge-sharing forums.Stakeholder Engagement & Communication

  • Act as the interface between the site C&Q teams, project management, and quality assurance functions.

  • Communicate progress, risks, and key decisions to stakeholders through clear reporting and status updates.

  • Support quality reviews by providing subject matter expertise and ensuring documentation readiness.
    Qualifications:Basic Qualifications- Bachelor’s degree in Engineering, Life Sciences, or a related technical field.

  • 7+ years of experience in commissioning, qualification, or validation in a GMP-regulated environment.

  • Demonstrated leadership experience, including direct people management or technical team leadership.
    Preferred Qualifications- Master’s degree in Engineering or related discipline.

  • Experience leading C&Q activities for large-scale capital projects (biotech, pharmaceutical, or sterile manufacturing preferred).

  • Strong understanding of ASTM E2500, ISPE Baseline Guides, GAMP principles, and FDA/EMA regulatory expectations.

  • Proven track record of implementing process improvements and standardization initiatives.

  • Excellent organizational, communication, and stakeholder management skills.

  • Ability to work effectively in a matrixed, cross-functional, and fast-paced environment.
    Competencies:- Strategic Thinking and Decision-Making

  • Technical Expertise in C&Q and Validation Science

  • Leadership and Talent Development

  • Continuous Improvement and Innovation

  • Collaboration and Influence

  • Project Management and Execution Excellence

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About Amgen

Amgen

A biotechnology company that develops and manufactures human therapeutics for various illnesses and diseases.

10,001+

Employees

Thousand Oaks

Headquarters

$138B

Valuation

Reviews

3.8

2 reviews

Work Life Balance

2.5

Compensation

3.0

Culture

3.0

Career

4.0

Management

3.0

70%

Recommend to a Friend

Pros

Professional development opportunities

Exposure to diverse functions and projects

Large-scale project experience

Cons

Understaffed with high output expectations

Limited permanent job opportunities

Temporary contract limitations

Salary Ranges

1,544 data points

L2

L3

L4

L5

L6

L2 · Financial Analyst L2

0 reports

$94,068

total / year

Base

$37,627

Stock

$47,034

Bonus

$9,407

$65,848

$122,288

Interview Experience

3 interviews

Difficulty

2.7

/ 5

Duration

14-28 weeks

Experience

Positive 0%

Neutral 33%

Negative 67%

Interview Process

1

Application Review

2

Recruiter Screen

3

Technical Phone Screen

4

Onsite/Virtual Interviews

5

Final Round Interview

6

Offer

Common Questions

Coding/Algorithm

Technical Knowledge

Behavioral/STAR

System Design

Past Experience