AL Solutions
Are you passionate about biopharmaceutical manufacturing and protein purification? We're looking for a
Downstream Manufacturing Scientist
to play a key role in purifying mammalian cell-based cultures and producing recombinant proteins for biosimilars at clinical and commercial scale.
Considering making an application for this job Check all the details in this job description, and then click on Apply.
This is a
hands-on position
within a GMP-compliant environment, focused on operating at the 50L–1000L scale. If you’re experienced with
AKTA purification skids, TFF systems, and downstream processing —and want to be part of an innovative team driving meaningful therapies to market—this could be your next career move.
What You’ll Do:
Execute downstream processes at multiple scales in a
GMP environment Operate
AKTA systems, TFF , and other purification equipment Perform
column packing , troubleshoot processes, and analyze data Lead or assist in
batch execution, protocols, and investigations Collaborate with cross-functional teams and vendors to resolve technical issues Support
GMP documentation , batch record creation, and regulatory compliance Contribute to
equipment maintenance
and EHS policy adherence
What We’re Looking For:
Bachelor’s or Master’s in
Chemical, Biological, or Biochemical Sciences 2+ years
of experience in biopharma manufacturing (GMP environment) Hands-on expertise with
AKTA Process skids , single-use systems, and downstream purification Familiarity with
batch records, GMP documentation , and aseptic techniques Strong problem-solving, communication, and teamwork skills
Bonus Points:
Experience with
engineering & clinical batch execution Working knowledge of
cleaning validation
and regulatory inspection readiness
Downstream Manufacturing Scientist
to play a key role in purifying mammalian cell-based cultures and producing recombinant proteins for biosimilars at clinical and commercial scale.
Considering making an application for this job Check all the details in this job description, and then click on Apply.
This is a
hands-on position
within a GMP-compliant environment, focused on operating at the 50L–1000L scale. If you’re experienced with
AKTA purification skids, TFF systems, and downstream processing —and want to be part of an innovative team driving meaningful therapies to market—this could be your next career move.
What You’ll Do:
Execute downstream processes at multiple scales in a
GMP environment Operate
AKTA systems, TFF , and other purification equipment Perform
column packing , troubleshoot processes, and analyze data Lead or assist in
batch execution, protocols, and investigations Collaborate with cross-functional teams and vendors to resolve technical issues Support
GMP documentation , batch record creation, and regulatory compliance Contribute to
equipment maintenance
and EHS policy adherence
What We’re Looking For:
Bachelor’s or Master’s in
Chemical, Biological, or Biochemical Sciences 2+ years
of experience in biopharma manufacturing (GMP environment) Hands-on expertise with
AKTA Process skids , single-use systems, and downstream purification Familiarity with
batch records, GMP documentation , and aseptic techniques Strong problem-solving, communication, and teamwork skills
Bonus Points:
Experience with
engineering & clinical batch execution Working knowledge of
cleaning validation
and regulatory inspection readiness