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Manufacturing, Training And Compliance Lead

EyePoint PharmaceuticalsNorthbridge, MA

$94,760 - $119,480 / year

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Overview

Schedule
Full-time
Education
Engineering (PE)
Career level
Senior-level
Remote
On-site
Compensation
$94,760-$119,480/year
Benefits
Career Development

Job Description

Manufacturing & Operations at EyePoint ensures the safe, compliant, and reliable production of innovative therapies for patients with serious retinal diseases. This team oversees end-to-end manufacturing, supply chain, and facilities with a strong focus on regulatory compliance, patient safety, and product integrity. Manufacturing & Operations strives to maintain rigorous standards and efficient processes with the goal of delivering safe, high-quality therapies to patients.

The MFG Training and Compliance lead will report to the AD of Manufacturing Training, Compliance and Operational Excellence and is responsible for the daily execution, coordination, and tracking of floor-level training programs and regulatory compliance activities. This role bridges the gap between regulatory requirements and plant floor operations, ensuring that all manufacturing personnel are fully qualified, compliant with cGMP/safety guidelines, and prepared for internal and external audits.

This is a site-based role supporting our Northbridge Manufacturing facility. Travel to our other MFG locations may be required to support a multi-site team.

Primary responsibilities include, but are not limited to, the following:

Individual Responsibilities

Training Execution & Coordination

  • On-the-Job Training (OJT): Coordinate and deliver technical on-the-job training and onboarding for manufacturing technicians and operators.
  • LMS Administration: Manage the site's Learning Management System (LMS) to assign courses, log completions, and generate qualification reports.
  • Competency Assessment: Conduct routine performance evaluations and practical exams to certify that operators can safely and accurately run production equipment.

Compliance Tracking & Audit Readiness

  • Curriculum Compliance: Monitor team training matrices daily to ensure no operator performs a task without active qualifications.
  • SOP & Documentation Review: Assist in writing, revising, and reviewing Standard Operating Procedures (SOPs), training logs, and logbooks to ensure they match current shop-floor practices.
  • Audit Support: Act as the primary point of contact for training documentation during regulatory inspections to quickly retrieve employee records.

Deviation & CAPA Support

  • Root Cause Analysis: Partner with Quality and Operations teams to investigate manufacturing deviations linked to human error or lack of training.
  • Preventive Actions: Design and implement specific training interventions as part of Corrective and Preventive Actions (CAPAs) to prevent issue recurrence.

Required Skills & Knowledge

Primary skills and knowledge required include, but are not limited to the following:

  • Ability to translate complex regulatory requirements and data trends into simple, actionable manufacturing workflows.
  • Experience with inspection readiness initiatives and in involvement with PAI inspections
  • Exceptional verbal and written communication skills to influence cross-functional stakeholders and present data to executive leadership.
  • Proven track record of systematically resolving root causes of operational and compliance issues.
  • Ability to work collaboratively in a fast-paced, dynamic work environment, while managing multiple priorities
  • Self-motivated, strong work ethic, strong organizational skills, strong communication skills, critical thinking, attention to detail and accuracy, the ability to work independently and in a team environment are essential
  • Flexible and able to respond quickly to shifting priorities and meet deadlines
  • Track record of strong personal performance combined with demonstrated ability to build and lead highly engaged teams in a high growth environment

Required Education & Experience

Level of Education Required:

  • Bachelor's degree in Engineering, Life Sciences, or a related technical field (or an equivalent combination of education and hands-on manufacturing experience).

Number of Years of Experience in the Function and in the Industry:

  • Minimum of 5 years of experience working in a highly regulated manufacturing environment (Pharmaceutical, Biotech, Medical Device, or Aerospace), with at least 2 years in a dedicated training, compliance, or coordinator capacity.

EyePoint is committed to fair and equitable compensation practices. The salary offer is commensurate with EyePoint's compensation philosophy and considers factors including but not limited to education, training, experience, market conditions, criticality of the role and internal equity. 

The target salary range for this position is listed below:

Salary Range

$94,760—$119,480 USD

Envision Your Future

With the exciting energy of a winning culture and an exhilarating pace, we are an ophthalmology company committed to preventing blindness by developing and commercializing innovative therapeutics.

The collective power of our values influences everything we do, and everything we do for you.

Transformational Innovation

We exist to change our patients' lives through the power of sight. We are forward looking, embrace challenges with curiosity, and continuously seek to improve our products and ourselves by learning, problem-solving and pushing the limits of science and technology.

Unwavering Integrity

We recognize our responsibility to our patients, employees, and our community, and value the trust they put in us. We set a high ethical bar and expect responsible leadership at every level to ensure we serve those who matter most to us.

Compassionate Excellence

We believe that fun and excellence can coexist. We foster a culture where enjoying the work we do and caring for each other are as important as delivering exceptional outcomes.

Inclusive Collaboration

We strive to see through the eyes of others and work as one team. We appreciate one another's differences and perspectives, and ensure everyone feels valued, respected and encouraged to bring their ideas forward.

EyePoint is proud to be an equal opportunity employer. We believe that diversity and inclusion among our colleagues is critical to our success as a company, and we seek to recruit, develop, and retain the most talented people from a diverse candidate pool. All applicants will be considered for employment without attention to age, race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.

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FAQs About Manufacturing, Training And Compliance Lead Jobs at EyePoint Pharmaceuticals

What is the work location for this position at EyePoint Pharmaceuticals?
This job at EyePoint Pharmaceuticals is located in Northbridge, MA, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at EyePoint Pharmaceuticals?
Candidates can expect a pay range of $94,760 and $119,480 per year.
What employment applies to this position at EyePoint Pharmaceuticals?
EyePoint Pharmaceuticals lists this role as a Full-time position.
What experience level is required for this role at EyePoint Pharmaceuticals?
EyePoint Pharmaceuticals is looking for a candidate with "Senior-level" experience level.
What education level is required for this job?
The education requirement for this position is Engineering (PE). Candidates with relevant qualifications or equivalent experience may also be considered.
What benefits are offered by EyePoint Pharmaceuticals for this role?
EyePoint Pharmaceuticals offers Career Development for this position. Actual benefits may vary depending on the employer's policies and employment terms.
What is the process to apply for this position at EyePoint Pharmaceuticals?
You can apply for this role at EyePoint Pharmaceuticals either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.