Job added in hotlist
Applied job
Contract job
Recruiter job
Employer job
Expanded search
Apply online not available
Similar Jobs
GEHC Technical Writer III
Abacus Service Corporation
Marlborough, MA
Apply Now >
GEHC Technical Writer III
The Ian Martin Group
Marlborough, MA
Apply Now >
Sr Advisor - Minute Clinic - Epic Clarity Report Writer
CVS Caremark.
Woonsocket, RI
Apply Now >
Staff Writer
Gannett Co., Inc.
Cambridge, MA
Apply Now >
MarComm Editor
The Hanover Insurance Group, Inc.
Worcester, MA
Apply Now >
View more jobs in Marlborough, MA
View more jobs in Massachusetts

Job Details

GEHC - Technical Writer III

Company name

Marlborough, MA

Apply for this job

13 hit(s)  


BCforward is seeking a highly motivated and experienced

Technical Writer III/

Technical Document Writer- Biomanufacturing

Title: Technical Writer III/

Technical Document Writer- Biomanufacturing

Duration: 6 Months

Location: Marlborough, MA 01752

Shift Timings: Monday Friday, 8:00am 4:30pm.

Function: Manufacturing

Job Description:

**Quality Assurance experience, Bio-pharmaceutical

Change controls and documentation.

Required Qualifications:

3 years of previous technical writing experience in a cGMP pharmaceutical environment.

Experience in manufacturing under cGMP guidelines and possess a strong knowledge of cGMP requirements.


We are currently looking for a cGMP Technical Writer who will be responsible for writing, reviewing and driving production and quality documentation to approval.

The Technical Document Writer will be responsible for producing high-quality cGMP documentation that contributes to the overall success of our project goals.

Additional responsibilities might include tracking of the daily, weekly and monthly forecasted documentation priorities required to meet output quotas.




Originate, revise and maintain Standard Operating Procedures (SOPs), Production Batch Records (PBRs) and Solution Preparation Records.

Compile and draft procedural documentation using standard electronic publishing tools.

Create and maintain templates for cGMP documents.

Collaborate with individuals from various internal functional areas to generate and review new equipment, processing, set-up and operational documents within agreed upon timelines.

Interview subject matter experts to obtain details in order to accurately capture content material.

Demonstrate effective written and verbal communication skills.

Monitor the flow of production documents and adjust workload and resources in an appropriate, organized and efficient manner.

Work with cross-functional teams on the implementation of process improvement initiatives to increase quality in cGMP documentation.

Demonstrate an ability to multi-task and manage multiple projects independently

Maintain a safe work environment for self and staff.

Quality Specific Goals:

Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position.

Complete all planned Quality & Compliance training within the defined deadlines.

Identify and report any quality or compliance concerns and take immediate corrective action as required.

Aware of and comply with Stop Order, Concessions, ESD ECO, Calibration, Preventative Maintenance, Material Identification & Segregation, and Good Documentation Practices, as associated with this job type/position.

Training: Aware of and comply with GEHC training requirements.

Required Qualifications:

3 years of previous technical writing experience in a cGMP pharmaceutical environment.

Experience in manufacturing under cGMP guidelines and possess a strong knowledge of cGMP requirements.

Prior experience working in a



Exceptional written/verbal communication, listening, organizational, interpersonal, research, investigative, and problem-solving skills.

Proven ability to communicate complex ideas in a clear, concise manner.

Working knowledge of MS Office Suite and an Electronic Document Management System (EDMS).

Experience with Document Proficiency in Microsoft Office Products.

Preferred Qualifications:

Associates degree in a scientific discipline or equivalent experience.

Cell Culture experience.

Protein Purification experience.

Biological Technical Transfer experience.

Contact Name:

Jai Sharma

How to Apply:

To apply for this posting please send your resume to


About BCforward



began as an IT business solutions and staffing firm. Founded in 1998, BC


has grown with our customers needs into a full service personnel solutions organization. Headquartered in Indianapolis, Indiana, BC


also operates numerous delivery centers across North America and India. We are currently the largest consulting firm and largest MBE certified firm in Indiana. Our uninterrupted growth has allowed BC


to deliver uniquely configured IT staffing and project solutions for over years of catering to our customers specific needs. BC


currently maintains a team of over 5000 global resources. With our additional brand, Stafforward, together we have the capabilities to deliver services for a variety of industries in both public and private sectors which allows us to address your most challenging needs.

Location/Region: Marlborough, MA (US)

Company info

Website :

Company Profile
At BCforward, adding value is a pillar of our mission. With our best-in-class strategic IT outsourcing, we leverage economies of scale and complementary core competencies to deliver cost effective, value-added solutions. BCforward strives for quality solutions, timely delivery, competitive price and an innovative approach. We achieve this through entrepreneurial attitude, business processes, project management, proven relationships and flexibility.

Similar Jobs:
Technical Content Writer
Location : Boston, MA
Technical Content Writer Lightwave Partners • Boston MA Job #641392530 As a Technical Content Strategist, you will be responsible for planning and writing the content to describe security risks and events, helping the team choose ...
Senior Medical Writer
Location : Belmont, MA
Senior Medical Writer Custom Learning Designs, Inc • Belmont MA Job #641392821 Senior Medical Writer If you thrive in an intellectually stimulating environment where you can combine your love for writing with your medical and scie...
Technical Document Writer
Location : Marlborough, MA
Technical Document Writer needed. Temporary and full-time role. Long-term ,12-month contract. Must have three plus years of technical writing experience. Manufacturing experience required. Prior pharmaceutical work exp. required. ...
I found a new job! Thanks for your help.
Thomas B - ,
  • All we do is research jobs.
  • Our team of researchers, programmers, and analysts find you jobs from over 1,000 career pages and other sources
  • Our members get more interviews and jobs than people who use "public job boards"
Shoot for the moon. Even if you miss it, you will land among the stars.
WritingCrossing - #1 Job Aggregation and Private Job-Opening Research Service — The Most Quality Jobs Anywhere
WritingCrossing is the first job consolidation service in the employment industry to seek to include every job that exists in the world.
Copyright © 2018 WritingCrossing - All rights reserved. 21