Technical Writer

  • Location
    Bedford, New Hampshire
  • Job type
    Contract/Temp to Hire
  • Category
    Office, Clerical & Administrative - Clerical

Adecco is searching for an experienced Technical Writer for a position in Bedford NH.

Primary responsibilities include:
-Conduct complex document generation and revision including batch production records
and manufacturing procedures.
-Technical writing of protocols, standard operating procedures and GMP batch records
(new and revisions) based on project scope and client processes.
-Perform review of manufacturing documentation generated by the receiving unit
(manufacturing records, SOPs, etc.).
-Support and develop consistent manufacturing standards for controlled documents used
within cGMP manufacturing
-Ensures all tasks are performed consistently with safety standards and cGMP guidelines.
-Management of document review and approval processes with cross functional teams.
-Under assignment from MTS management sit on tech transfer teams learning client
processes and act as a technical liaison with the client and other MTS team members.
-Assist with supporting MTS Engineers and Manufacturing Operation leads in generation
of project documentation (i.e. material control procedures, training manuals).
-Compose quality system reports (unplanned deviation investigations, CAPA support) as
requested from MTS management.
-Participate in study teams and investigations (internal and external).
-Floor support of technical operations as requested from MTS senior staff.
-Review batch records for compliance and improvement as required, focusing specifically
on: processing parameters, materials, equipment use.
-Basic compliance knowledge, analytical and troubleshooting skills to support
manufacturing operations.


Minimum Requirements:
-Associates Degree in a Life Science/Technical Field or BS/BA Degree with relevant
technical/science knowledge.
-Process development or production experience preferred with basic understanding of
(Chemistry, Math and laboratory sciences)
-BS in a science field desirable.
-Demonstrable knowledge of GLP/GMP, in particular manufacturing and/or laboratory
practices and quality systems.
-Strong technical writing skills preferred and ability to work with cross functional team.
-Minimum of 2 years? experience in an industry where technical/scientific writing was
performed.
-Experience in a GMP industry in a manufacturing documentation support area desirable.
-Excellent communication skills, drive, sense of urgency, energy level and problem-solving
abilities.
-Proven experience with strong organizational and interpersonal skills.
-Ability to work independently in a cross functional environment.
-Capability working within a matrix/dynamic environment would be advantageous.
-While performing the duties of this job, the employee may be required to sterile gown as
needed for ISO and aseptic environments.

If you are interested in this role please call us at 603-598-0117 or hit apply now to be considered!

  • Apply with Adecco

Reference number US_EN_1_025281_11809063