1 Message
Digest #3451
Message
Wed Jan 6, 2016 9:45 am (PST) . Posted by:
"Edith Paul"
Please contact the recruiter if interested.
Thank you.
---------- Forwarded message ----------
From: Elise Martin <emartin@mutualtargetinc.com>
Date: Wed, Jan 6, 2016 at 8:47 AM
Subject: Position Description QA Compliance Official
To: paul.edith@gmail.com
Cc: emartin@mutualtargetinc.com, lwinchek@mutualtargetinc.com
Hello again Edith! Here is the description for a *permanent position* you
may be interested in as QA Compliance Official for a Pharmaceutical /
Biotech company located in Stillwater, PA. *If you are not already working
with another recruiter and have not applied directly to Sanofi in the last
6 months*, please review the description and send me your most recent
resume in Word file doc format. I will be contacting you with a few
questions if you feel this position may be a good fit. Have a wonderful
day meanwhile.
Thank you!
Elise Martin
(Sanofi) QA Compliance Official
Swiftwater, PA
QA Compliance Official
*Position Summary:*
Ensure compliance with cGMP, regulatory and internal requirements regarding
the manufacturing, testing and distributing of products through formal QA
Audits, investigations, training and recommendations to procedures.
*Position Responsibilities:*
Evaluate and provide Quality Assurance recommendations on all products,
processes, systems and deficiencies that are/may be affected by regulatory
or cGMP requirements
Ensure compliance with applicable regulatory requirements, to be in a
constant state of inspection readiness
Complete incident investigations in response to any unexplained events
encountered during manufacturing or out-of-specification lab results for
functional areas
Provide input, guidance and recommendations to department management
regarding results of investigation and process improvements
Provide cGMP audits of processing areas
Monitor observations and address all concerns
* Key Competencies and Soft-Skills*
Strong communication, interpersonal, teamwork and organization skills
A good understanding of vaccines/biologics products and associated
technologies
Strength in several LEAD Competences-Think Strategically, Lead Teams, Act
for Change, Strive for Results, Cooperate Transversally, Commit to
Customers, Make Decisions
*Who You Are*
You are inspired and driven by the company mission to improve worldwide
human health. You would fit in well with the values of innovation,
solidarity, confidence, respect and integrity and our ways of working
(Focus, Agility, Accountability and Simplicity).
Our company is an Equal Opportunity and Affirmative Action employers
committed to a culturally diverse workforce. All qualified applicants will
receive consideration for employment without regard to race, color,
religion, sex, national origin, disability or protected veteran status, or
any other characteristics protected by applicable law.
#LI-sp
Qualifications
Basic Qualifications:
•Bachelor's Degree in life sciences.
•Minimum 5 years' experience in a cGMP controlled/pharmaceutical industry
(specific to Quality assurance experience)
Primary Location: United States-Pennsylvania-Swiftwater
*Compensation*
Base Salary - $80,000 to $95,000
Benefits - Full
Relocation Assistance Available - Yes
Commission Compensation - No
Bonus Eligible - Yes
Overtime Eligible - No
Interview Travel Reimbursed - Yes
*Candidate Details*
*5+ to 7 years experience*
Management Experience Required - No
Minimum Education - Bachelor's Degree
Willingness to Travel - Occasionally
*Additional Details*
Location: Swiftwater
Industry: Pharmaceutical / Biotech
Job Category: Manufacturing - Quality
Hours Per Week:
Visa Candidate Considered: No
*Elise Martin*
*Mutual Target Associates Recruiter*
EMartin@MutualTargetInc.com
Office Hours 9am – 5pm CST
Phone: 646 467-6772
Thank you.
---------- Forwarded message ----------
From: Elise Martin <emartin@mutualtargetinc.com>
Date: Wed, Jan 6, 2016 at 8:47 AM
Subject: Position Description QA Compliance Official
To: paul.edith@gmail.com
Cc: emartin@mutualtargetinc.com, lwinchek@mutualtargetinc.com
Hello again Edith! Here is the description for a *permanent position* you
may be interested in as QA Compliance Official for a Pharmaceutical /
Biotech company located in Stillwater, PA. *If you are not already working
with another recruiter and have not applied directly to Sanofi in the last
6 months*, please review the description and send me your most recent
resume in Word file doc format. I will be contacting you with a few
questions if you feel this position may be a good fit. Have a wonderful
day meanwhile.
Thank you!
Elise Martin
(Sanofi) QA Compliance Official
Swiftwater, PA
QA Compliance Official
*Position Summary:*
Ensure compliance with cGMP, regulatory and internal requirements regarding
the manufacturing, testing and distributing of products through formal QA
Audits, investigations, training and recommendations to procedures.
*Position Responsibilities:*
Evaluate and provide Quality Assurance recommendations on all products,
processes, systems and deficiencies that are/may be affected by regulatory
or cGMP requirements
Ensure compliance with applicable regulatory requirements, to be in a
constant state of inspection readiness
Complete incident investigations in response to any unexplained events
encountered during manufacturing or out-of-specification lab results for
functional areas
Provide input, guidance and recommendations to department management
regarding results of investigation and process improvements
Provide cGMP audits of processing areas
Monitor observations and address all concerns
* Key Competencies and Soft-Skills*
Strong communication, interpersonal, teamwork and organization skills
A good understanding of vaccines/biologics products and associated
technologies
Strength in several LEAD Competences-Think Strategically, Lead Teams, Act
for Change, Strive for Results, Cooperate Transversally, Commit to
Customers, Make Decisions
*Who You Are*
You are inspired and driven by the company mission to improve worldwide
human health. You would fit in well with the values of innovation,
solidarity, confidence, respect and integrity and our ways of working
(Focus, Agility, Accountability and Simplicity).
Our company is an Equal Opportunity and Affirmative Action employers
committed to a culturally diverse workforce. All qualified applicants will
receive consideration for employment without regard to race, color,
religion, sex, national origin, disability or protected veteran status, or
any other characteristics protected by applicable law.
#LI-sp
Qualifications
Basic Qualifications:
•Bachelor's Degree in life sciences.
•Minimum 5 years' experience in a cGMP controlled/pharmaceutical industry
(specific to Quality assurance experience)
Primary Location: United States-Pennsylvania-Swiftwater
*Compensation*
Base Salary - $80,000 to $95,000
Benefits - Full
Relocation Assistance Available - Yes
Commission Compensation - No
Bonus Eligible - Yes
Overtime Eligible - No
Interview Travel Reimbursed - Yes
*Candidate Details*
*5+ to 7 years experience*
Management Experience Required - No
Minimum Education - Bachelor's Degree
Willingness to Travel - Occasionally
*Additional Details*
Location: Swiftwater
Industry: Pharmaceutical / Biotech
Job Category: Manufacturing - Quality
Hours Per Week:
Visa Candidate Considered: No
*Elise Martin*
*Mutual Target Associates Recruiter*
EMartin@MutualTargetInc.com
Office Hours 9am – 5pm CST
Phone: 646 467-6772
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