Sr. Process Engineer

Reposted 6 Days Ago
Be an Early Applicant
Fenton, MO, USA
In-Office
Senior level
Healthtech • Pharmaceutical • Telehealth
The Role
The Sr. Process Engineer improves safety, quality, and productivity in pharmaceutical manufacturing, ensuring compliance and enhancing processes through continuous improvement.
Summary Generated by Built In

Why Us?

At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.

Job Description Summary

The Sr. Process Engineer serves as main point of contact for manufacturing processes regarding safety, quality, and continuous improvement activities. Improves safety, quality, and productivity of a solid dose pharmaceutical operation. Consistently seeks for and evaluates methods to improve overall customer satisfaction through improved manufacturing efficiencies.

Job Description

ESSENTIAL FUNCTIONS:

  • Works closely with Research & Development (R&D) organization project managers and formulators for new product transfer into the facility.
  • Identifies and implements improvements to existing processes using continuous improvement tools.
  • Ensures that processes comply with all cGMP regulations in regards to process and cleaning validation.
  • Completes exception investigations and implements effective corrective and preventative actions.
  • Write and update batch records for new and existing product lines.
  • Ensures accurate completion of all paperwork and documentation including batch records, equipment, etc.
  • Design, validate and commission new production equipment and tooling, monitor modifications and upgrades, and troubleshoot existing processes.
  • Write and execute validation documentation (process, cleaning, and equipment) for new and existing product lines.
  • Regular participation in production daily operations meeting and lead team problem solving efforts.
  • Work with plant safety to maintain process specific safety information.
  • Assist in developing training programs and/or SOPs to enhance skills sets and reduce defects.
  • Support customer or regulatory agency audits as the subject matter expert for assigned processes.
  • Provide technical support and problem resolution.
  • Ensuring that process critical maintenance is completed in a timely manner to reduce downtime
  • Candidate may also have to assist in production efforts when necessary.
  • Coordinate projects as assigned.
  • Perform other duties as assigned.

MINIMUM REQUIREMENTS:

Education:

BS degree in Industrial, Manufacturing, Chemical Engineering or related field.

Experience:

Five years of related experience in pharmaceutical industry.  Solid dose production experience is preferred

Preferred Skills/Qualifications:

Strong knowledge of chemistry, physics, and engineering principles.

Experience with manufacturing processes.

Ability to effectively communicate with all levels of the organization, from operations to senior management, both oral and written format

Other Skills:

Knowledge of cGMP regulations.

Excellent communication skills, both oral and written

Strong working knowledge of Microsoft Office products including Word and Excel

RELATIONSHIPS WITH OTHERS:

The Sr. Process Engineer supports the pharmaceutical manufacturing process and may be assigned a general plant support role.  Position interacts with production technicians, production managers, project managers and Leadership team member, R&D, corporate engineering and external vendors

WORKING CONDITIONS:  Works an equal amount of time on the production floor in a manufacturing environment and an office type environment.  The time spent on the production floor may be extended periods of time within a manufacturing facility

DISCLAIMER:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification.  They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of employees assigned to this position.

EEO Statement:

We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. 

Skills Required

  • BS degree in Industrial, Manufacturing, Chemical Engineering or related field
  • Five years of related experience in pharmaceutical industry
  • Strong knowledge of cGMP regulations
  • Excellent communication skills, both oral and written
  • Strong working knowledge of Microsoft Office products including Word and Excel

Endo Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Endo and has not been reviewed or approved by Endo.

  • Fair & Transparent Compensation Pay is considered competitive to good across many roles, with total compensation in commercial positions strengthened by sizable bonus/OTE when targets are met. Subsidiary experiences within the group also point to good compensation, reinforcing a generally positive pay story.
  • Healthcare Strength Core medical, dental, and vision coverage is strong, complemented by virtual care, disease‑management programs, and a health advocate service. Health coverage is described as good, adding perceived value beyond base pay.
  • Retirement Support A 401(k) plan provides a company match up to 4%, supporting employees’ long‑term savings. Current materials outline the matching formula clearly for prospective comparisons.

Endo Insights

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The Company
Montreal, Quebec
1,722 Employees
Year Founded: 1997

What We Do

At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs. Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward. Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life. Endo has global headquarters in Malvern, Pennsylvania. Community Guidelines: 1. Be respectful. Everyone who visits our page should feel comfortable and respected. 2. If we see a comment that violates anything in the following list, it may be removed. • Comments that use profanity; personally attack or bully another individual; or are off-topic, misleading, factually inaccurate, political, spam, defamatory, discriminatory or promotional. • Comments that are excessively repetitive and/or disruptive to the community. • Comments that promote illegal activity, use copyrights or trademarks or are related to an ongoing legal matter. • Comments that appear to be medical advice. We reserve the right to remove a reply for any reason at any time. 3. Adverse Event Reporting: If we see a post about an adverse event, an Endo representative will need to contact you to find out more information to comply with regulatory guidelines. If you experience a side effect while using an Endo product, please consult your physician or pharmacist immediately. You may also report to the FDA at fda.gov/medwatch or 800-FDA-1088. Replies from other users do not necessarily reflect the views of Endo. We do not endorse content added by other users.

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