MES Process Engineer / Senior Process Engineer - 5052

Posted 19 Days Ago
Be an Early Applicant
Boston, MA
70K-113K Annually
Mid level
Pharmaceutical
The Role
The MES Process Engineer will support the MES Syncade system within manufacturing processes, optimize workflows, design experiments, manage CAPAs, draft technical reports, and guide junior team members. The role involves ensuring compliance and effective communication within teams and clients.
Summary Generated by Built In

Description

Verista’s 600 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

Company Culture Guidelines & Values:

  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise

MES Process Engineer Responsibilities:

  • Serve as the primary support for the MES Syncade system, ensuring its seamless integration with manufacturing processes
  • Develop a deep understanding of manufacturing workflows to optimize and enhance processes with MES
  • Review Functional Requirement Specifications (FRS) and test scripts for alignment with manufacturing
  • Independently design experiments and evaluate data in support of improvements and investigations
  • Support failure investigations and implementation of solutions (CAPAs) that solve manufacturing and product problems, follow up on CAPAs to determine effectiveness and suitability and prepare/review written reports in a timely fashion
  • Draft technical reports in support of manufacturing process changes, optimizations, and regulatory filings
  • Provide technical guidance and leadership to lesser experienced team members
  • Ensure maintenance/ required control of records of qualification and validation, Change Controls, Risk Assessments and CAPAs for future compliance audits
Requirements
  • The ideal candidate must have knowledge of process manufacturing, field instrumentation, control system installation and implementation expertise in all of the following project phases: Requirements documentation, detailed design generation, implementation, system integration, testing and on-site startup. Plans and coordinates technical design and engineering implementation of project work
  • 4 - 6 years of role relevant experience
  • Strong understanding of biological process validation activities including drug substance manufacturing processes, drug product filling processes, process simulations (media fills), filtration, mixing, sterilization, lyophilization, and completion of validation risk assessments and evaluations
  • Ability to mentor and guide lesser experienced team members
  • Ability to communicate effectively with clients
  • Proven ability to identify areas of business expansion and report to management team for follow-up
  • Strong understanding of the three stages of Process Validation: Process Design, Quality Control, and Continuous Process Verification
  • Obvious business maturity and interpersonal skills to be able to effectively communicate and collaborate
  • Experience and capability of effectively communicating requirements (written and orally) with rationale to different levels of the client’s organization
  • Intermediate Microsoft Project capabilities
Benefits

Why Choose Verista?

  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • As Needed Sick Time
  • Tuition Reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Parental Leave and Bereavement

For more information about our company, please visit us at 

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

$70,491-112,515

*Verista is an equal opportunity employer.

The Company
HQ: Fishers, IN
402 Employees
On-site Workplace
Year Founded: 2020

What We Do

Verista is a leading business and technology consultancy firm that provides systems, compliance, validation and quality solutions to life science companies - enabling them to improve health and improve lives. We help clients solve their most critical and complex challenges across the GxP lifecycle, from preclinical and clinical to commercialization, manufacturing and distribution – bringing together decades of knowledge, the most advanced engagement platforms and transformative technologies. This allows clients to benefit from the ease, efficiency and trust that results from working with one partner who excels across specialties. Verista’s clients trust the company’s 650+ experts to deliver consistent, safe, and high-quality results across the product development lifecycle. Verista is based in Fishers, Indiana, Wayne, Pennsylvania, Westford, Massachusetts, and San Mateo, California. For more information, visit www.verista.com

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