Steri-Pharma
Quality Assurance Analyst (QA/QC), 2nd/3rd Shift, Pharma
Steri-Pharma, Syracuse, New York, us, 13235
Quality Assurance Analyst (QA/QC), 2nd/3rd Shift, Pharma
2nd/3rd Shift (Monday-Thursday, 4x10-hour shifts 3:00pm-1:30am; shift premium provided), schedule flexibility required. Initial training will take place on 1st Shift.
Join Our Talent Community
Our growth is real and we're looking for the best of the best who are committed to making a difference. We want people who are enthusiastic, rigorous, collaborative, and confident in teams. Above all, we want people who share our fundamental core values - quality, reliability, meeting customer needs, integrity, respect for each other, and collaboration.
Our employees enjoy a wide array of benefits designed to provide safety and security for themselves and their families. We are proud of the benefit programs we provide, including:Exceptional healthcare insurance100% match 401k plan and immediate vesting!Incredible time-off plan (because family is important), up to 5 weeks to start (vacay +sick + holiday)Many fun events throughout the year!How this position makes a difference:
This position performs environmental monitoring and quality control of aseptic process area, to include testing of components according to established procedures. Position reviews records for accuracy. Position applies standard concepts, practices, and procedures within the laboratory. Position performs a variety of tasks related to both Quality Assurance and Quality Control.
Your responsibilities:
Performs occasional environmental monitoring in areas of varying aseptic classification.Performs data entry and prepares various reports.Completes Batch Record Reviews.Completes tagging of material.Maintains and orders supplies in assigned areas.Performs laboratory maintenance.Performs Logbook reviews as required.Performs equipment and area purges as necessary.Maintains attention to detail while reviewing records, logbooks, and issuance of records.Assists with special projects as required or requested.Promote a safe and harmonious work environment.Maintain compliance with SOPs, GMPs, and all company policies.Other duties as assigned or required.You bring these qualities:
A Bachelor's degree from a regionally accredited institution in science or related field.At least 1-3 years' experience in a laboratory setting.Knowledge of contemporary laboratory practices and procedures.Knowledge and skill in operating various specialized equipment.Knowledge of general computer functions such as Microsoft Office programs, spreadsheets, etc.Skill in handling several projects or tasks at the same time, or within a given time frame.Advanced Problem Safety Sensitivity; the ability to recognize a safety issue or potential safety issue.Skill to use time management techniques in personal daily tasks and that of others.Ability to apply critical thinking.Advanced interpersonal and communication skills.Ability to maintain confidentiality of all internal and external information and processes.Ability to follow personal hygiene standards/procedures according to SOP.Ability to wear protective attire as required and don gowning materials in correct order per SOP.Ability to follow all appropriate SOPs and safety procedures per company guidelines.Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.Ability to be flexible in work hours.Ability to provide motivational support.Ability to maintain a professional, positive attitude at all times.Ability to trust, develop, maintain, and strengthen partnerships with others inside the organization who can provide information, assistance, and support.Ability to lead by example.Ability to communicate with coworkers, management team members, and other individuals in a courteous and professional manner.Ability to work in a fast paced environment.Ability to pay close attention to detail and coordinate various activities simultaneously.Ability to complete assigned tasks.Expectations:
Projects are completed on time and per documented project plansYou are well trained, cooperative, work collaboratively, and maintain GMP complianceReports are completed accurately and in a timely mannerMaintain a positive attitude and be helpful at all timesValue personal competency and the competency of co-workersBe receptive to constructive feedbackGowns according to proceduresMaintains confidentialityMaintains required hygieneMaintains a work environment that is safe and healthy and meets regulatory standardsMeets departmental standardsMeets goals established by your managerCo-workers and peers describe you as positive and collaborativeAttends work as scheduledAct as a role model within and outside the companyPhysical Dimensions:
Seeing: Must be able to read reports and use computer 75-100% of timeHearing: Must be able to hear well enough to communicate with coworkers 75-100% of timeStanding/Walking/Mobility: Must be able to stand to open files and operate office equipment; mobility between departments and attend meetings of coworkers and management 75-100% of timeClimbing/Stooping/Kneeling: Must be able to climb, stoop, or kneel to perform routine tasks within the scope of job 50-74% of timeLifting up to 50 lbs./Pulling/Pushing within the scope of job 25-49% of timeTouching/Grasping/Feeling: Must be able to write, type, and use office equipment; along with handling material and equipment 75-100% of time
All requirements are subject to possible modification to reasonably accommodate individuals with disabilities. The above statements are intended to describe the general nature and level of work being performed. This document in no way states or implies that these are the only duties to be performed by the employee occupying this position. Employees will be required to follow any other job-related instructions and to perform any other job-related duties requested by their supervisor.
**Please note: this job posting is for the 2nd/3rd Shift, Quality Assurance Analyst (QA/QC) role. If you are interested in another position and/or shift, please apply to the relevant job posting. **
About Us: https://www.steri-pharma.com
Notice of Employee Rights, Protections, and Obligations under Labor Law Section 740: https://dol.ny.gov/system/files/documents/2022/02/ls740_1.pdf
EEOC 'Know Your Rights' Poster: https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf
Employee Rights Under the Polygraph Protection Act: https://www.dol.gov/sites/dolgov/files/WHD/legacy/files/eppac.pdf
2nd/3rd Shift (Monday-Thursday, 4x10-hour shifts 3:00pm-1:30am; shift premium provided), schedule flexibility required. Initial training will take place on 1st Shift.
Join Our Talent Community
Our growth is real and we're looking for the best of the best who are committed to making a difference. We want people who are enthusiastic, rigorous, collaborative, and confident in teams. Above all, we want people who share our fundamental core values - quality, reliability, meeting customer needs, integrity, respect for each other, and collaboration.
Our employees enjoy a wide array of benefits designed to provide safety and security for themselves and their families. We are proud of the benefit programs we provide, including:Exceptional healthcare insurance100% match 401k plan and immediate vesting!Incredible time-off plan (because family is important), up to 5 weeks to start (vacay +sick + holiday)Many fun events throughout the year!How this position makes a difference:
This position performs environmental monitoring and quality control of aseptic process area, to include testing of components according to established procedures. Position reviews records for accuracy. Position applies standard concepts, practices, and procedures within the laboratory. Position performs a variety of tasks related to both Quality Assurance and Quality Control.
Your responsibilities:
Performs occasional environmental monitoring in areas of varying aseptic classification.Performs data entry and prepares various reports.Completes Batch Record Reviews.Completes tagging of material.Maintains and orders supplies in assigned areas.Performs laboratory maintenance.Performs Logbook reviews as required.Performs equipment and area purges as necessary.Maintains attention to detail while reviewing records, logbooks, and issuance of records.Assists with special projects as required or requested.Promote a safe and harmonious work environment.Maintain compliance with SOPs, GMPs, and all company policies.Other duties as assigned or required.You bring these qualities:
A Bachelor's degree from a regionally accredited institution in science or related field.At least 1-3 years' experience in a laboratory setting.Knowledge of contemporary laboratory practices and procedures.Knowledge and skill in operating various specialized equipment.Knowledge of general computer functions such as Microsoft Office programs, spreadsheets, etc.Skill in handling several projects or tasks at the same time, or within a given time frame.Advanced Problem Safety Sensitivity; the ability to recognize a safety issue or potential safety issue.Skill to use time management techniques in personal daily tasks and that of others.Ability to apply critical thinking.Advanced interpersonal and communication skills.Ability to maintain confidentiality of all internal and external information and processes.Ability to follow personal hygiene standards/procedures according to SOP.Ability to wear protective attire as required and don gowning materials in correct order per SOP.Ability to follow all appropriate SOPs and safety procedures per company guidelines.Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.Ability to be flexible in work hours.Ability to provide motivational support.Ability to maintain a professional, positive attitude at all times.Ability to trust, develop, maintain, and strengthen partnerships with others inside the organization who can provide information, assistance, and support.Ability to lead by example.Ability to communicate with coworkers, management team members, and other individuals in a courteous and professional manner.Ability to work in a fast paced environment.Ability to pay close attention to detail and coordinate various activities simultaneously.Ability to complete assigned tasks.Expectations:
Projects are completed on time and per documented project plansYou are well trained, cooperative, work collaboratively, and maintain GMP complianceReports are completed accurately and in a timely mannerMaintain a positive attitude and be helpful at all timesValue personal competency and the competency of co-workersBe receptive to constructive feedbackGowns according to proceduresMaintains confidentialityMaintains required hygieneMaintains a work environment that is safe and healthy and meets regulatory standardsMeets departmental standardsMeets goals established by your managerCo-workers and peers describe you as positive and collaborativeAttends work as scheduledAct as a role model within and outside the companyPhysical Dimensions:
Seeing: Must be able to read reports and use computer 75-100% of timeHearing: Must be able to hear well enough to communicate with coworkers 75-100% of timeStanding/Walking/Mobility: Must be able to stand to open files and operate office equipment; mobility between departments and attend meetings of coworkers and management 75-100% of timeClimbing/Stooping/Kneeling: Must be able to climb, stoop, or kneel to perform routine tasks within the scope of job 50-74% of timeLifting up to 50 lbs./Pulling/Pushing within the scope of job 25-49% of timeTouching/Grasping/Feeling: Must be able to write, type, and use office equipment; along with handling material and equipment 75-100% of time
All requirements are subject to possible modification to reasonably accommodate individuals with disabilities. The above statements are intended to describe the general nature and level of work being performed. This document in no way states or implies that these are the only duties to be performed by the employee occupying this position. Employees will be required to follow any other job-related instructions and to perform any other job-related duties requested by their supervisor.
**Please note: this job posting is for the 2nd/3rd Shift, Quality Assurance Analyst (QA/QC) role. If you are interested in another position and/or shift, please apply to the relevant job posting. **
About Us: https://www.steri-pharma.com
Notice of Employee Rights, Protections, and Obligations under Labor Law Section 740: https://dol.ny.gov/system/files/documents/2022/02/ls740_1.pdf
EEOC 'Know Your Rights' Poster: https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf
Employee Rights Under the Polygraph Protection Act: https://www.dol.gov/sites/dolgov/files/WHD/legacy/files/eppac.pdf