Technical Writer II - Canton
Company: Fagron GmbH & CO. KG
Location: Boston
Posted on: November 13, 2024
Job Description:
Over de functieAbout the Job:Perform Manufacturing investigative
writing and technical writing, including but not limited to change
controls, protocols, reports, and/or standard operating
procedures/manufacturing batch records. The position requires
working with minimal supervision to manage assigned tasks from
initiation to completion. This is a desk job which may require you
to stay seated for 6+ hours.Independently responsible for the
efficient and thorough investigation of process deviations,
determination of root cause, and initiation of
corrective/preventative actions designed to adequately address and
correct the Quality related deficiencies identified during the
investigation process. Responsible to provide proactive corrections
based on noted trends to minimize the potential for repeat
incidents that may lead to, or result in, impact to product or
patient/operator safety.Responsibilities:
- Independently responsible for the efficient and thorough
investigation of process deviations, determination of root cause,
and initiation of corrective/preventative actions designed to
adequately address and correct the Quality related deficiencies
identified during the investigation process.
- As part of each investigation, gathers information from all
necessary internal and external sources in order to evaluate the
impact of the deviation on previously manufactured product, as well
as the risk to future operations.
- Prepares and analyzes historical data and uses methodical
root-cause analysis tools to determine and effectively communicate
root causes.
- Responsible for ensuring compliance with relevant Standard
Operating Procedures, while gathering, analyzing and applying
information from internal and external sources in order to perform
a risk assessment of the impact each process deviation has on the
product, process, and patient health and safety.
- Responsible to provide proactive corrections based on noted
trends to minimize the potential for repeat incidents that may lead
to, or result in, impact to product or patient/operator
safety.
- Provides technical expertise to the site to ensure that
investigation corrective and preventative actions are complete,
thorough, accurate, and timely.
- Updates and maintains all related quality management systems in
compliance with various governing procedures and policies as they
relate to investigations and performs trend analysis.
- Works independently to comply with procedure driven guidelines
relating to Deviation and complaint investigations and makes
decisions that directly affect patient health and safety.
- Demonstrates strong technical skills; provides technical
assistance to area supervisors or managers to solve complex
problems.
- Ensures that deadlines are maintained and closely monitors the
need for extensions to be administered in relation to Subsequent
Actions and Investigations in order to maintain compliance in this
area.
- Perform any other tasks/duties as assigned by Manufacturing
Management.Wat wij vragen
- BA/BS Degree in science field, e.g., Biology, Microbiology,
Chemistry, Pharmacy, etc. or equivalent combination of education
and experience.
- At least three years' experience in a GMP manufacturing
environment. Must be familiar with regulatory (FDA)
requirements.
- Minimum 2 years experience with performing and documenting
investigations and/or authoring standard operating procedures.
- Advanced writing skills, including experience with root cause
analysis tools.
- Good deductive and inductive critical thinking skills with
attention to detail and ability to manage multiple projects with
shifting priorities.
- Must possess strong interpersonal, written, and verbal
communication skills. Candidate must be able to interface
positively with Regulatory Agencies, vendors, and company
departments.
- Proficient in MS Office programs, including Word and
Excel.
- Prefer candidates proficient with MasterControl QMS.Wat wij
biedenWe believe in our people and foster a supportive environment
that develops and rewards performance and incentivizes long-term
career success. Our benefits include, but are not limited to:
- Competitive Salary
- Health, Vision, and Dental Insurance
- Company Paid Life Insurance
- Generous Paid Holidays
- Paid Volunteer Time
- Generous Paid Time Off and Rollover
- Company matching 401K and Retirement Savings Plans
- Employee Assistance Program
- Flexible working arrangementsNow let's not forget our site!The
FSS Boston facility is in beautiful Canton, Massachusetts.
Employees enjoy ample parking at a state-of-the-art compounding
facility. The employee breakroom provides plenty of storage for
lunches and you can enjoy free coffee anytime of the day!Fagron US
is committed to creating a diverse environment and is proud to be
an equal opportunity employer. All qualified applicants will
receive consideration for employment without regard to race; creed;
color; religion; national origin; sex; age; disability; sexual
orientation; gender identity or expression; genetic predisposition
or carrier status; veteran, marital, or citizenship status; or any
other status protected by law. Fagron US is proud to be an
affirmative action and equal opportunity employer.Over het
bedrijfFagron was founded in Rotterdam (The Netherlands) in 1990
and is a dynamic organization with over 3,000 employees worldwide.
As the global market leader in personalized medicine, we are highly
passionate about being at the forefront of our field. Each day, we
are committed to improving the lives of millions of people across
the world by optimizing and innovating personalized pharmaceutical
solutions.If you would like to be part of such an important
challenge and feel you would thrive among dedicated and passionate
colleagues, then chances are you will discover a career at Fagron
that you'll love! Together we create the future of personalizing
medicine.
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Keywords: Fagron GmbH & CO. KG, Quincy , Technical Writer II - Canton, Advertising , Boston, Massachusetts
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