Top 11 Pharmaceutical deviation writer Jobs

Deviation Writer
INCOG BioPharma Services —Fishers, IN
- Full-time
- Mid-level
- Office
- 3 years
QA Investigations / Technical Writer
KVK Tech —Newtown, PA
- Mid-level
- 3 years
- Master's degree
- Paid holidays
- Dental insurance
Production Investigator/Technical Writer
Indivior —Raleigh, NC
- Full-time
- Bachelor of Science
- Mid-level
- Associate's degree
- Profit sharing
- Employee stock purchase plan
Principal Associate - QA
Lilly —Indianapolis, IN
- $65,250 - $169,400 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
9d
Quality Systems Specialist
Blood Bank of Alaska, Inc. —Anchorage, AK
- Full-time
- Microsoft Excel
- Mid-level
- Ability to climb stairs
- Health insurance
- Dental insurance
Quick Apply
Senior QA Associate
KVK Tech —Newtown, PA
- Analysis skills
- Senior level
- Leadership
- Paid holidays
- Dental insurance
Study Physician, Oncology (Remote)
BI Pharmaceuticals, Inc. —Ridgefield, CT
- Full-time
- Remote
- 18 years or older
- Medicine
- Pass drug screening
Director, Manufacturing Operations
Fresenius Kabi —Melrose Park, IL
- $190,000 - $225,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Analysis skills
- Wellness program
- Paid holidays
Clinical Research Coordinator / Madison, WI (On-Site)
Fortrea —Madison, WI
- Full-time
- Mid-level
- Clinic
- Mentoring
- Disability insurance
- Health insurance
14d
Associate Process Development Scientist/Engineer 1
CEDENT —United States
- Full-time
- Microsoft Excel
- 6 years
- ERP systems

More jobs to discover

Find similar jobs that you might be interested in.

Pharmaceutical Technical Writer
ProStaff Solutions Inc —New Brunswick, NJ
Work with process owners and SMEs to implement agreed upon procedural documentation and to develop cross-functional process models. Travel Estimate: Up to 5%.
Quick Apply
Quality Lab Associate II, Chemistry
Hikma Pharmaceuticals PLC —Cherry Hill, NJ
Exceptional organizational skills and ability to plan and implement resolutions to technical problems. Provide support to Chemistry laboratory as technical…
$44,900 - $74,950 a year
Quick Apply

I want to receive the latest job alert for pharmaceutical deviation writer

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

pharmaceutical deviation writer jobs near

Quality Specialist jobs in Anchorage, AK

Technical Writer jobs in Raleigh, NC

Technical Writer jobs in Newtown, PA

Writer jobs in Fishers, IN

Quality Assurance Analyst jobs in Indianapolis, IN

Senior Quality Assurance Associate jobs in Fall River, Ma

Associate Degree Computer Science jobs in New Jersey

Senior Quality Assurance Associate jobs in Denver, Co

Senior Quality Assurance Associate jobs in Berkeley Heights, Nj

Senior Quality Assurance Associate jobs in Long Beach, Ca

Sunrise Senior Living jobs in Kennebunk, Me

Quality Analyst jobs in Houston, Tx

Quality Specialist jobs in Hummelstown, Pa

Environmental Health Specialist jobs in California

Quality Specialist jobs in Rock Hill, Sc

Remote Clinical Documentation Specialist jobs in Wisconsin

Quality Specialist jobs in Morrisville, Nc

Quality Specialist jobs in Wisconsin

Technical Writer jobs in Mckinney, Tx

Technical Writer jobs in Omaha, Ne

Deviation Writer

INCOG BioPharma Services
Fishers, IN

Apply Now

Job Details

Full-time

Qualifications

Content creation for technical audiences
Technical documentation
Technical writing within manufacturing
GMP

Full Job Description

Job Description

INCOG BioPharma Services is seeking an experienced and detail-oriented Deviation Writer to join our Manufacturing Engineering team. This role is crucial for translating a variety of complex technical events into clear, accurate, and robust investigations. The Deviation Writer will work closely with the Manufacturing, Production Engineering, Manufacturing Sciences and Technology, Supply Chain, Quality, and other cross-functional teams to create comprehensive investigations that leverage facts and data to support robust root cause conclusions, effective corrective actions, and systematic all-encompassing preventative actions. The Deviation Writer will exemplify excellent interpersonal skills and be capable of developing productive customer-centric working relationships with internal and external customers and have a role with high visibility to all departments. The Deviation Writer will have strong familiarity with industry standard electronic Quality Management System(s) and Microsoft Office suite products.

They will thrive working autonomously utilizing strong self-management and organization skills but also be able to interact, collaborate, and lead within a team environment. The Deviation Writer will value the processes owned by internal customers and subject matter experts and will possess a demonstrated ability to support and influence positive outcomes in the application of that knowledge to wider processes.

Essential Job Functions:

Understand, investigate, and author a variety of deviating conditions or nonconforming events across multiple technical departments, in alignment with Subject Matter Experts.
Self-motivated to fact gather, analyze information, interpret data, utilize expertise from Subject Matter Experts, etc. in an effort to provide supportive evidence to the investigation and root cause.
Experience utilizing a variety of analysis tools to support root cause identification; Ishikawa Fishbone, 5 Why, etc.
Ability to critically think outside the box for robust corrective and preventative actions; leveraging automation and engineering controls to error-proof equipment and processes.
Demonstrated ability to translate complex, technical processes and descriptions into simplified, understandable write ups.
Eagerness to collaborate and partner with both internal and external stakeholders to comprehensively represent the facts of an investigation in a logical and presentable manner.
Evaluating historical deviating conditions, adverse events, non-conformances, etc. in order to identify and prevent trends.

Special Job Requirements:

Bachelor’s degree in a scientific, engineering, or technical discipline.
Minimum of 3 years of experience in technical writing within a regulated GMP environment, preferably in the pharmaceutical, biopharmaceutical, or biotechnology industries.

Additional Preferences:

Proficient in writing clear, concise, and accurate technical documentation.
Strong understanding of GMP manufacturing processes and regulatory requirements.
Excellent organizational skills with high attention to detail.
Ability to collaborate effectively with cross-functional teams and communicate complex information to diverse audiences.
Familiarity with documentation tools and electronic document management systems (EDMS).
Exceptional computer skills, particularly moderate to expert level experience with Microsoft Word and Microsoft Excel.

Additional info about INCOG BioPharma Services:

At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.

If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.

Apply Now

Refine Your Search

pharmaceutical deviation writer jobs

Deviation Writer

QA Investigations / Technical Writer

Production Investigator/Technical Writer

Principal Associate - QA

Quality Systems Specialist

Senior QA Associate

Study Physician, Oncology (Remote)

Director, Manufacturing Operations

Clinical Research Coordinator / Madison, WI (On-Site)

Associate Process Development Scientist/Engineer 1

More jobs to discover

I want to receive the latest job alert for pharmaceutical deviation writer

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected