Process Alliance
Overview
We’re hiring a deviation writer to join a pharmaceutical manufacturing team in Durham, North Carolina. This full‑time, on‑site role is ideal for an
early‑career scientist or engineer
with 1–2 years of experience in GMP manufacturing or quality support.
Key Responsibilities
Write detailed deviation reports, documenting investigations in compliance with GMP standards
Collaborate with cross‑functional teams (QA, manufacturing, QC, engineering) to gather data and support root cause analysis
Ensure timely closure of deviations and support CAPA documentation as needed
Participate in deviation trending and reporting to drive continuous improvement
Qualifications
Bachelor’s degree in a scientific or engineering or related field
1–2 years of experience in the pharmaceutical industry
Experience writing or supporting GMP deviation investigations preferred
Packaging experience
is a plus
Quality Control Lab experience
is a plus but not required
Strong analytical and writing skills
Familiarity with quality systems is a plus
About Our Culture At Process Alliance, we strive to be a better model for how problems are solved, and solutions are delivered. We believe in providing a supportive and inclusive work environment where employees can thrive both personally and professionally. Join our team and be part of a company that is shaping the future of engineering solutions.
Visit our website at www.processalliance.com to explore our projects, expertise, and the impact we make in the engineering and consultancy space.
Benefits
Medical insurance
Vision insurance
401(k)
Paid maternity leave
Paid paternity leave
Process Alliance is an equal opportunity employer. We encourage applications from candidates of all backgrounds and experiences.
Salary: $120,000.00–$125,000.00 annually. Location: Durham, NC. Current: posted 3 days ago.
Job Details Seniority level:
Associate
Employment type:
Full‑time
Job function:
Consulting and Engineering
Industries:
Pharmaceutical Manufacturing
#J-18808-Ljbffr
early‑career scientist or engineer
with 1–2 years of experience in GMP manufacturing or quality support.
Key Responsibilities
Write detailed deviation reports, documenting investigations in compliance with GMP standards
Collaborate with cross‑functional teams (QA, manufacturing, QC, engineering) to gather data and support root cause analysis
Ensure timely closure of deviations and support CAPA documentation as needed
Participate in deviation trending and reporting to drive continuous improvement
Qualifications
Bachelor’s degree in a scientific or engineering or related field
1–2 years of experience in the pharmaceutical industry
Experience writing or supporting GMP deviation investigations preferred
Packaging experience
is a plus
Quality Control Lab experience
is a plus but not required
Strong analytical and writing skills
Familiarity with quality systems is a plus
About Our Culture At Process Alliance, we strive to be a better model for how problems are solved, and solutions are delivered. We believe in providing a supportive and inclusive work environment where employees can thrive both personally and professionally. Join our team and be part of a company that is shaping the future of engineering solutions.
Visit our website at www.processalliance.com to explore our projects, expertise, and the impact we make in the engineering and consultancy space.
Benefits
Medical insurance
Vision insurance
401(k)
Paid maternity leave
Paid paternity leave
Process Alliance is an equal opportunity employer. We encourage applications from candidates of all backgrounds and experiences.
Salary: $120,000.00–$125,000.00 annually. Location: Durham, NC. Current: posted 3 days ago.
Job Details Seniority level:
Associate
Employment type:
Full‑time
Job function:
Consulting and Engineering
Industries:
Pharmaceutical Manufacturing
#J-18808-Ljbffr