Manufacturing Associate
PMRS Inc PMRS Inc Horsham, PA Horsham, PA Full-time Full-time $80,000 - $100,000 a year $80,000 - $100,000 a year 7 days ago 7 days ago 7 days ago PMRS Inc.
provides cGMP contract manufacturing and analytical services from early clinical development to commercial production.
PMRS Inc.
's streamlined processes facilitate timely production of the highest quality products at the lowest possible cost.
PMRS is an ISO 9001, ISO 14001,and ISO 27001 company.
Website:
http:
//www.
pmrsinc.
com
Job Description:
We are open to both recent graduates as well as those already in employment who are looking for a change who are hardworking and have the ability to learn and adapt.
Responsibilities at this position will include following batch records and using manufacturing equipment to manufacture various finished pharmaceutical products.
Some of the jobs and equipment that individuals will work on include raw materials dispense, blenders with Process Analytical Technology (PAT), tablet presses, fluid beds, roller compactors, granulators, extruders, capsule fillers, coaters and printers.
In addition to working on manufacturing production lines, the individuals will be responsible for all of the support around a cGMP facility including equipment qualification, maintenance, calibration and cleanliness of all equipment utilized throughout the processes.
Individuals will be involved in the review of standard operating procedures, batch records and documentation in order to support the processing.
Keys to Success Must be a self-starter and capable of working with minimal oversight Ability to work with their hands and various types of equipment Ability to problem solve Create value for the position, department and company Proactive Quality by Design, not reactive auditing, root cause analysis Must understand and participate in prevention and be able to improve systems and procedures as applicable Must be able to work in a fast paced and changing environment and know how to prioritize activities appropriately Must understand and participate in prevention and be able to improve systems and procedures as applicable Must understand quality Education& Experience Requirements Preferred a Bachelor's Degree in a related field to an accredited US college or university Salaried employees are compensated for a 50 hour work week Background and Credit Check required as part of the hiring process Job Type:
Full-time Pay:
$80,000.
00 - $100,000.
00 per year
Benefits:
401(k) 401(k) matching Dental insurance Health insurance Health savings account Life insurance Paid time off Vision insurance Schedule:
10 hour shift Monday to Friday Application Question(s):
What is your definition of quality? Give me an example of a time where you worked with your hands.
Will you pass a background check? Education:
Bachelor's (Preferred) Work Location:
In person We are open to both recent graduates as well as those already in employment who are looking for a change who are hardworking and have the ability to learn and adapt.
Responsibilities at this position will include following batch records and using manufacturing equipment to manufacture various finished pharmaceutical products.
Some of the jobs and equipment that individuals will work on include raw materials dispense, blenders with Process Analytical Technology (PAT), tablet presses, fluid beds, roller compactors, granulators, extruders, capsule fillers, coaters and printers.
In addition to working on manufacturing production lines, the individuals will be responsible for all of the support around a cGMP facility including equipment qualification, maintenance, calibration and cleanliness of all equipment utilized throughout the processes.
Individuals will be involved in the review of standard operating procedures, batch records and documentation in order to support the processing.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
provides cGMP contract manufacturing and analytical services from early clinical development to commercial production.
PMRS Inc.
's streamlined processes facilitate timely production of the highest quality products at the lowest possible cost.
PMRS is an ISO 9001, ISO 14001,and ISO 27001 company.
Website:
http:
//www.
pmrsinc.
com
Job Description:
We are open to both recent graduates as well as those already in employment who are looking for a change who are hardworking and have the ability to learn and adapt.
Responsibilities at this position will include following batch records and using manufacturing equipment to manufacture various finished pharmaceutical products.
Some of the jobs and equipment that individuals will work on include raw materials dispense, blenders with Process Analytical Technology (PAT), tablet presses, fluid beds, roller compactors, granulators, extruders, capsule fillers, coaters and printers.
In addition to working on manufacturing production lines, the individuals will be responsible for all of the support around a cGMP facility including equipment qualification, maintenance, calibration and cleanliness of all equipment utilized throughout the processes.
Individuals will be involved in the review of standard operating procedures, batch records and documentation in order to support the processing.
Keys to Success Must be a self-starter and capable of working with minimal oversight Ability to work with their hands and various types of equipment Ability to problem solve Create value for the position, department and company Proactive Quality by Design, not reactive auditing, root cause analysis Must understand and participate in prevention and be able to improve systems and procedures as applicable Must be able to work in a fast paced and changing environment and know how to prioritize activities appropriately Must understand and participate in prevention and be able to improve systems and procedures as applicable Must understand quality Education& Experience Requirements Preferred a Bachelor's Degree in a related field to an accredited US college or university Salaried employees are compensated for a 50 hour work week Background and Credit Check required as part of the hiring process Job Type:
Full-time Pay:
$80,000.
00 - $100,000.
00 per year
Benefits:
401(k) 401(k) matching Dental insurance Health insurance Health savings account Life insurance Paid time off Vision insurance Schedule:
10 hour shift Monday to Friday Application Question(s):
What is your definition of quality? Give me an example of a time where you worked with your hands.
Will you pass a background check? Education:
Bachelor's (Preferred) Work Location:
In person We are open to both recent graduates as well as those already in employment who are looking for a change who are hardworking and have the ability to learn and adapt.
Responsibilities at this position will include following batch records and using manufacturing equipment to manufacture various finished pharmaceutical products.
Some of the jobs and equipment that individuals will work on include raw materials dispense, blenders with Process Analytical Technology (PAT), tablet presses, fluid beds, roller compactors, granulators, extruders, capsule fillers, coaters and printers.
In addition to working on manufacturing production lines, the individuals will be responsible for all of the support around a cGMP facility including equipment qualification, maintenance, calibration and cleanliness of all equipment utilized throughout the processes.
Individuals will be involved in the review of standard operating procedures, batch records and documentation in order to support the processing.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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