QC Technical Writer (3-Month Contract) (Philadelphia)
AL Solutions, Philadelphia, PA, United States
QC Technical Writer (3-Month Contract) | GMP | Onsite
I’m currently partnered with a
biologics-focused CDMO
who are continuing to scale their GMP operations as they move towards commercial readiness across the US. As part of this growth, they are looking to bring on a
QC Technical Writer
on an
initial 3-month contract , with strong likelihood of extension.
The Role
This position will focus on supporting the QC and Analytical teams with
technical documentation , ensuring all methods, protocols, and reports are clearly written, compliant, and inspection-ready. You’ll play a key role in bridging
science and documentation , working closely with QC, Analytical Development, and QA teams.
Key responsibilities include: Authoring and editing
analytical methods, protocols, and technical reports Supporting documentation related to
method qualification and validation Reviewing and improving existing QC documentation for clarity and compliance Ensuring all documentation aligns with
GMP and regulatory standards Collaborating with QC, Analytical Development, and QA teams Supporting documentation for
technology transfer and commercial readiness
What They’re Looking For Experience working in a
GMP-regulated environment
(pharma, biotech, CDMO) Strong background in
technical writing within QC or Analytical Development Experience with
analytical methods, validation, or laboratory documentation Excellent written communication skills with strong attention to detail Ability to translate complex scientific data into clear, compliant documentation
Why This Role? Join a company undergoing
significant GMP expansion and commercial growth High-impact role supporting
QC and analytical readiness for manufacturing Work closely with scientific teams in a
highly collaborative environment Fast-moving process with
immediate start available Strong potential for extension beyond the initial
3-month contract
If this sounds interesting, feel free to apply or message George Higginson directly for a confidential discussion.
I’m currently partnered with a
biologics-focused CDMO
who are continuing to scale their GMP operations as they move towards commercial readiness across the US. As part of this growth, they are looking to bring on a
QC Technical Writer
on an
initial 3-month contract , with strong likelihood of extension.
The Role
This position will focus on supporting the QC and Analytical teams with
technical documentation , ensuring all methods, protocols, and reports are clearly written, compliant, and inspection-ready. You’ll play a key role in bridging
science and documentation , working closely with QC, Analytical Development, and QA teams.
Key responsibilities include: Authoring and editing
analytical methods, protocols, and technical reports Supporting documentation related to
method qualification and validation Reviewing and improving existing QC documentation for clarity and compliance Ensuring all documentation aligns with
GMP and regulatory standards Collaborating with QC, Analytical Development, and QA teams Supporting documentation for
technology transfer and commercial readiness
What They’re Looking For Experience working in a
GMP-regulated environment
(pharma, biotech, CDMO) Strong background in
technical writing within QC or Analytical Development Experience with
analytical methods, validation, or laboratory documentation Excellent written communication skills with strong attention to detail Ability to translate complex scientific data into clear, compliant documentation
Why This Role? Join a company undergoing
significant GMP expansion and commercial growth High-impact role supporting
QC and analytical readiness for manufacturing Work closely with scientific teams in a
highly collaborative environment Fast-moving process with
immediate start available Strong potential for extension beyond the initial
3-month contract
If this sounds interesting, feel free to apply or message George Higginson directly for a confidential discussion.