Sr tech lead - mfg. process planning

Hcl Technologies; Orlando (FL); On-site; USD 80,000 - 122,000; Full time

Job summary

An established industry player is seeking a Sr Process Validation Engineer to lead complex validation activities in manufacturing. This role involves ensuring compliance with regulations and validation policies while serving as a subject matter expert. The ideal candidate will have a strong background in medical device or pharmaceutical manufacturing and a passion for quality assurance. Join a dynamic team where your expertise will drive critical projects and contribute to the success of innovative solutions in the industry.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

401(k)

Paid Time Off

Life Insurance

Disability Insurance

Employee Assistance Programs

Qualifications

• 5-9 years of experience in medical device or pharmaceutical manufacturing.
• Expertise in validation processes and compliance with regulations.

Responsibilities

• Facilitates complex validation activities ensuring compliance with regulations.
• Acts as a technical expert and represents the project in validation meetings.

Skills

Manufacturing Process Planning

Process Validation

Education

Bachelor’s Degree in Science, Engineering, or Business

Master’s Degree

Job description

Project role: Sr tech lead - manufacturing process planning

Skills: Manufacturing Process Planning

• Secondary Skills: Process Validation

No. of positions: 1

Pay Range: $80,000 - $122,000

Job Title: Sr Process Validation Engineer

Location: Jacksonville, FL

Job Description:

• Facilitates complex validation activities within product, process, equipment, software, and facilities changes, ensuring compliance with regulations and validation policies.
• Represents the project in validation meetings, change control, and project teams as needed.
• Compiles data and reports to the project team periodically.
• Supports updates to quality documentation and procedures.
• Works independently on complex issues, serving as a subject matter expert in validation.
• Acts as a technical expert within the job function.
• Prioritizes tasks to meet deadlines.

Resource Requirements:

• Bachelor’s Degree in Science, Engineering, or Business; Master’s degree preferred.
• 5-9 years of industry experience in medical device or pharmaceutical manufacturing, Quality Assurance, or Regulatory fields.

Compensation and Benefits:

The salary will depend on location, skills, experience, and education. The role may include performance bonuses and benefits such as medical, dental, vision, pharmacy, life insurance, disability insurance, employee assistance programs, 401(k), paid time off, and holidays.

Disclaimer:

HCLTech is an equal opportunity employer. Concerns about discrimination can be reported to [e-mail].