Randstad Enterprise
Manufacturing (Parenteral) Technical Writer
Randstad Enterprise, Durham, North Carolina, United States,
Technical Writer I - Manufacturing Technical Operations-Parenteral FacilityOnsite contract role with Randstad at pharmaceutical manufacturing client in RTPMon-Fri 8-5 Pay rate: $32.00/hour 12 month contract
This role incorporates manufacturing documentation creation and revision, master production records (MPRs) and procedures, focused on supporting manufacturing operations.
RESPONSIBILITIES1.Creates and revises processes in procedures and work instructions independently and with collaboration from Quality Assurance and Manufacturing2. Coordinates document approval and issuance timing and communicates any issues to multiple cross-functional groups.3. Works to identify continuous improvement opportunities related to the MFG process.-Identifies issues and resolutions as it relates to established MFG processes-Sits on teams to help with identifying improvement opportunities and helps to brainstorm and execute solutions.-Plans and executes work with supervision using on the job experience and existing precedents and procedures to resolve simple problems or issues in a given area and works with significant oversight in complex situations.-Identifies/troubleshoots technical problems that are simple in nature.-Ability to facilitate meetings with cross functional teams
PREFERRED SKILLSHighly proficient in MS WordTechnical writingPrevious Parenteral Vial Filling experience a plus
EDUCATION/QUALIFICATIONSMinimum: High School DiplomaPreferred: associate or bachelor's degree or equivalent skilled trades or vocational training.Other educational levels accepted based on related experience 0 - 2+ years (depending on educational and industry experience type)This position will provide opportunities to collaborate and innovate with groups of individuals who are all passionate about transforming patient lives!Randstad offers health insurance benefits and if you feel this might be a good fit for you, apply now and let's schedule a time to discuss to move forward.
This role incorporates manufacturing documentation creation and revision, master production records (MPRs) and procedures, focused on supporting manufacturing operations.
RESPONSIBILITIES1.Creates and revises processes in procedures and work instructions independently and with collaboration from Quality Assurance and Manufacturing2. Coordinates document approval and issuance timing and communicates any issues to multiple cross-functional groups.3. Works to identify continuous improvement opportunities related to the MFG process.-Identifies issues and resolutions as it relates to established MFG processes-Sits on teams to help with identifying improvement opportunities and helps to brainstorm and execute solutions.-Plans and executes work with supervision using on the job experience and existing precedents and procedures to resolve simple problems or issues in a given area and works with significant oversight in complex situations.-Identifies/troubleshoots technical problems that are simple in nature.-Ability to facilitate meetings with cross functional teams
PREFERRED SKILLSHighly proficient in MS WordTechnical writingPrevious Parenteral Vial Filling experience a plus
EDUCATION/QUALIFICATIONSMinimum: High School DiplomaPreferred: associate or bachelor's degree or equivalent skilled trades or vocational training.Other educational levels accepted based on related experience 0 - 2+ years (depending on educational and industry experience type)This position will provide opportunities to collaborate and innovate with groups of individuals who are all passionate about transforming patient lives!Randstad offers health insurance benefits and if you feel this might be a good fit for you, apply now and let's schedule a time to discuss to move forward.