Paonta Sahib, Himachal Pradesh



In-process monitoring and analysis of Manufacturing & Packing activities of Tablets and Capsules.

Ensure compliance to cGMP Regulations, established SOPs, FO/MI and PO/PI and for all operational activities, area and equipment.

Perform QA review of executed batch production records and ensure the submission of Batch production record in the document cell.

Calibration & maintaining documentation of In-process Quality Assurance (IPQA) instruments.

Data back-up activities of IPQA instruments as per defined SOP frequency.

Monitor the environmental conditions mentioned in the batch production record and SOP.

Certification of batch production records for compliance and stage-wise compliance.

Reporting any GMP related discrepancies, non-conformances and deviations to superiors immediately.

Collection and entry of data for APR preparation.

Imparting training to team members and subordinates.


Line Clearance:

Ensure physically that the area and equipment to be used for manufacturing and packaging of next product/batch are free from any material/remnants of previous product.

Ensure to prevent mix up and cross contamination.

Check for proper environmental conditions with respect to temperature, Relative humidity, differential pressure etc.

Ensure that the Batch Production record is completed up to the previous stage.

Verify the material with respect to the container labels and quantity from the batch production record.


In-Process Checks:

Ensure the calibration of instruments for in-process checks.

In-process checks as per the approved manufacturing and packaging instructions.

Enclose all the printouts generated during in-process checks along with the batch production record.

All printouts shall be duly signed after checking.

Inform the production manager, supervisor and quality assurance manager about the in-process failure observed during in-process checks.

To record all the observations in the Batch Production Record

Inspection:

Inspection of the Tablets/Capsules as per SOP.

Inspection of the Finished Goods as per SOP and clearance of Transfer Ticket by ensuring the quantity and batch details.

Sampling:

Ensure for usage of appropriate sampling tool for sampling.

Ensure sampling device cleaning prior to the sampling.

Bengaluru, Karnataka

Establishment and Sustenance Quality Management System
Part Qualification methodology for all major sub-assemblies
Support and implementation of documentation for Quality Manual and Operating Procedures, Quality Development Plan, CP, PPAP documentations, Part/process Check Lists and work Corrective Instructions and Technical Information Publication records.
Ensure 100% adherence to Quality of materials, Processes and Finished Goods.
Responsible for Process certification of critical characteristics at supplier and in-house.
Tracking & sustenance of implementation of changes in product/ process change note.
Process modification: Support and coordinate prototype qualification and implementation with Industrial Engineering and Manufacturing.
Monitoring of Measuring devices and test equipment and keeping track of Calibration.
Resolution action for Non-conformance reports for process and material.
Quality Verification with the stipulated suppliers and in-house activities.
Drive actions for reduction of Cost of poor quality and ensure Zero escapes.
All Process Revalidation and Recertification audits.
Support Supplier Evaluation with Sourcing department.
Support and coordinate prototype qualification and implementation
Participation in Job site visits to monitor the health of Factory supplies.
Resolving of issues related to product and processes
Otis is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.

Lexington, NC 27295
Full-time

Job Description:
What will you do?

This position will be responsible for product testing on specific assigned PCS (Power Control Systems) units and ensure that it is fully tested in accordance with ASCO procedures and standard industry practices testing the individual PCS sections, interconnecting the sections and testing the systems and the control programs. Also responsible to demonstrate the assigned PCS switchgear for customers during onsite witness tests. Position includes hands-on testing and troubleshooting with testers and design engineers.

Test, troubleshoot, correct and document wiring and functional problems in accordance with the wiring diagram.
Setup and perform PCS testing based on Sequence of Operation.
Interface with both production and engineering personnel to properly record and correct both physical and design nonconformance issues.
Configure and test PLC’s (Programmable Logic Controller) and power management networks.
Upload firmware and download parameters to control modules and other electronic components.
Set up electronic components and protective relays per vendor manuals.
Develop and build test simulations for customized PCS switchgear.
Serve as “technical” point person for test group on an assigned PCS unit
In order to meet customer demands, the position is subject to daily and weekend overtime to complete PCS Projects.
Position works within standard PCS operating procedures and guidelines.
Position requires a moderate degree of supervision.
Promote a safe work environment.
Performs other duties as assigned by supervisor.

QUALIFICATIONS:

Knowledge of electrical principals and power management.
Ability to read and follow schematics of complex electrical and mechanical circuits.
Knowledge of PLC interface and WonderWare programming strongly preferred.
Computer programming and networking skills are a strong plus.
2-year Associates Degree in Power, Electronics, Computer Networking with 2-3 years relative experience; or 4 years of Military Training in Power, Electronics or Computer Networking.

Bloomington, IN
Full-time

Summary

The Quality Associate II Line Operations is a member of the Quality Assurance Line Operations Team reporting directly to the Quality Supervisor. They maintain quality oversight of the manufacturing areas by working closely with manufacturing personnel and performing various checks during the manufacturing processes. They also assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Baxter Standard Operating Procedures. They facilitate training of new Quality Associates in QALO. This position strives for continuous improvement of processes and contributes to creating an environment where teamwork, productivity, safety, identity, strength, purity and quality (SISPQ) are reflected in the finished product.


Essential Duties and Responsibilities

Facilitates training qualifications and on-going support for associates, including activities such as aseptic intervention oversight, room inspections, oversight checklists, and equipment chart review
Leads cross functional continuous improvement project teams applying Lean principles
Serves as principal Quality author for Significant Nonconformance (potential batch impact) Reports
Provides technical support and guidance to nonconformance authors
Acts as team leader to shift associates in absence of supervisor
Assists supervisor in maintenance of visual controls and accountability tools
Ensures compliance with all federal, state, local and company-specific regulations related to quality of product and employee safety.
Reviews records to ensure they are complete, accurate and follows current Good Manufacturing Practices (cGMP) requirements. Records include batch records and other documents involved in the aseptic processing of drug product.
Reports errors, deficiencies, discrepancies and observations to management. May stop operations when product safety is or may be compromised.
Performs Quality functions in classified areas, including checklists, and aseptic intervention oversight.
Works in collaboration with management team to prepare for internal and external audits. Assists with timely closure of audit observations.
Authors Nonconformance Reports, Risk Assessments, and corrective action responses for exception variances.
Initiates standard operating procedure (SOP) revisions as needed to support continuous improvement.
Ensures that SOPs are current and effective and that staff performs routine tasks according to SOP through direct observation.

Minden, NE 68959
Full-time

Full Job Description

The Quality Assurance Specialist coordinates corrective action process and the resolution and elimination of nonconforming product.

Utilize MRB process (Defect Review) to assign immediate action for a proactive response to quality related issues.
Issue and assign internal corrective actions to responsible parties and follow up to ensure the timely closure of actions and coordinate the verification to ensure the corrective actions are effective.
Create and maintain a plan to close any nonconformance through further improvements to resolve the nonconformances.
Maintain the hold tag database and follow up to ensure resolutions to defective product are implemented and escalate as needed where further product impact is identified.
Maintain the status of work orders under investigation with the ERP system.
Develop a plan that identifies defective product at the point of inspection, and continually improve the integrity of data being collected.
Provide a basis for performance indicators to engineering.
Create metrics of performance for the area.
Internal Audits
Develop a plan, maintain, and monitor the performance continuously.
Ability to maintain regular, punctual, and reliable attendance as set by the supervisor according to handbook guidelines consistent with the ADA, FMLA and other federal, state and local standards.

Ennis, TX 75119
Full-time

Full Job Description

General Description


The responsibilities of the Quality Assurance Technician will include:

Conduct hourly production line audits to evaluate compliance to product standards, food safety standards and regulatory requirements. Document audit data.
Perform routine product tests during audits including: temperature, pH, oxygen, CEM moisture, net weight, particle size, vacuum, and packaging integrity to determine conformance to standards.
Be familiar with Freshpet HACCP programs for all products. Conduct and/or verify required HACCP food safety tests.
Perform product organoleptic evaluations on all pet food batches produced for conformance to standards. Document test results.
Work with operations to evaluate nonconformance occurrences and implement corrective action. Document data on Corrective Action Log.
Isolate and place nonconforming products or ingredients on hold and document hold by entering data on Hold Log and circulating information to Operations and Quality Management.
Inspect incoming ingredients for conformance to ingredient specifications, collect representative samples for testing and document audit data.
Collect routine product, ingredient or water samples for microbiological or chemical testing, shelf life evaluations or to use as retention samples.
Conduct Vacuum Tank Packaging tests on Roasted Meals, Vital Complete Meals and Single Serve products to evaluate packaging and seal integrity.
Test diluted sanitizers and foot bath solutions to verify concentration. Record data
Audit sanitation and perform ATP hygiene tests on food contact surfaces and equipment to determine sanitation effectiveness. Document swab data.
Take swab and sponge samples from established locations to evaluate plant Micro conditions. Record data.
Test cooling water for sanitary conditions and add biocides as need to control water quality. Record test data and chemical addition levels.
Monitor plant TPR tests and collect required samples for testing.
Provide technical support to Shift Supervisors and Line Leaders.
Assumes additional related responsibilities as necessary.
Any trained or qualified individual will serve as back up to this position.


Work Experience Requirements


Minimum 2 years’ experience working in Food Safety/Quality Systems, preferably in food or pet food.
Capable of performing and understanding mathematic calculations. Understanding of ratios, percentages, and fractions.
Basic understanding of Biology and/or Chemistry and associated technical terms.
Basic computer skills to read and write emails and enter data on spreadsheets.
Basic understanding of food Good Manufacturing Practices
Capable of following instructions and conducting routine Quality Assurance tests.
Good interpersonal and communication skills
Sound ethics


Education Requirements


High School Diploma or equivalent required.
Associate Degree in Science Area preferred.

Clarksburg, WV
Full-time

Education

Education may not be substituted for SE at either grade level.

Major Duties

Serves as an Examiner in a specialized quality assurance (QA) program, providing QA for functional areas of an assigned section
Performs assignments related to the verification, validation, audit, and consultative activities to ensure that QA and proficiency testing programs in use are producing quality products
Serves as a resource for the section and conducts periodic reviews to determine conformance with approved quality assurance policies and procedures
Recommends the implementation of corrective actions to ensure non-recurrence of deficiencies
Applies statistical QA and related methods to identify the sources of quality problems for specific functions and evaluates the effects proposed changes may have

San Diego, CA On-site

Full-time · Entry level
1,001-5,000 employees · Civil Engineering

Kleinfelder's San Diego office seeks experienced Construction Materials Testing Technicians with verified CALTRANS experience to join our team. Kleinfelder offers:

Competitive Wages;
Benefits, including medical, dental, vision, & life insurance; HSA & FSA; 401K; paid holidays; and paid time off (PTO);
Certification training and professional development (ICC, ACI, AWS, CalTrans, etc.);
Employee referral bonuses;
Career advancement opportunities with one of the largest and most respected firms in the industry.

We're looking for individuals with strong initiative, who will perform construction observation and materials testing on various projects to verify conformance to construction plans and specifications.

Specific responsibilities include:

following proper procedures,
completing work in a timely manner,
prepare daily field observation reports and materials testing data sheets
performing accurate computations, and
maintaining cordial relationships with coworkers, clients, contractors, etc.

This position may require travel from time to time.

Consideration for this position requires that following certifications or experience:

2 years minimum of construction materials testing or inspection experience.
1 year minimum of CALTRANS testing experience
Any combination of CALTRANS 125, 231, 504, 518, 533, and/or 539 certifications
Radiation Safety training for the operation of a nuclear density gauge.
High school diploma or equivalent.
Valid driver"s license with good driving record.
Able to use a company provided laptop or tablet computer and a working knowledge of MS Office programs (e.g. Word, Excel, Outlook, etc.).
A good work ethic and high level of personal integrity.
Authorization to work in the United States

Bengaluru, Karnataka


Job Description

The Global Quality Assurance (“QA”) Advisor position provides supports to ExxonMobil Global Business unit Product Quality Systems by conducting laboratory quality assurance assessments, providing expert quality assurance and laboratory methods consulting advice, and working with external organizations to improve industry laboratory and quality standards. QA Advisors are required to interface with local laboratory staff, Business unit Product Quality Advisors, Corporate Auditors, and external organizations. Global QA Advisors interact with the Global EMBSI(ExxonMobil Biomedical Sciences, Inc) team to implement the business unit lab assessment program and provide technical consulting support.

Job Role Responsibilities

Assess whether a laboratory is in compliance with quality control procedures and standards or not.
Assess both ExxonMobil and third-party contract laboratories against internal as well as industry standards including ISO 17025.
Conduct assessments at laboratory sites or remotely through desk-top or video audits as required; travel requirement is typically 50%.
Examine laboratory standards, procedures, test methods, and testing equipment for conformance to requirements. Accurately pinpoint issues in documentation, data quality, and performance through the assessment.
Prepare well written assessment reports documenting the assessment, compliance status, and recommendations for enhancing the quality system.
Lead assessment preparation, progress, and close-out meetings with staff and management as required. Assist laboratory staff with audit follow-up when required.
Coordinate with auditing teams and ensure excellent communications between teams and laboratory management.
Assist in the development of the assessment schedule and plan. Assist in the development of annual budgets for assigned assessment areas.
Provide professional and technical input for enhancements to data integrity and quality systems.
Provide quality assurance technical support and consulting to laboratories as required.


Job Requirements

Strong knowledge of product quality assurance systems and methods including ISO 17025.
Solid experience with auditing tools such as control charts and statistical methods related to test methods and data.
ISO 17025 Lead Auditor Certification.
HUET (Helicopter Underwater Escape Training) Certification, or the ability to complete HUET training course.
Strong ability to effectively manage working time and schedule.
Strong attention to detail, analytical, and problem solving ability.
Exceptional presentation, listening, and communication skills.
Ability to work effectively with all levels of the organization.
Able to work effectively as part of a diverse team of auditors and independently.
Ability to communicate fluently in both oral and written English. Must efficiently write technical reports and effectively present the information related to assessments.
Strong ability to coach and educate team members and laboratory staff.
Excellent hearing and vision required for normal assessment conversations, receiving information, and performing inspections.
Must have the ability to travel to and move about offices and laboratories around the Company.
Must be computer literate and proficient in commonly available software including MS Word, Excel, Access, and PowerPoint.
Bachelor’s degree with three or more years of internal auditing experience is desirable.
Oil and Chemical industry laboratory and manufacturing experience
ASQ(American Society for Quality)certifications are desirable
Effective communication in languages in addition to English preferred

Bengaluru, Karnataka

Job Description

The Global Quality Assurance ('QA') Advisor position provides supports to ExxonMobil Global Business unit Product Quality Systems by conducting laboratory quality assurance assessments, providing expert quality assurance and laboratory methods consulting advice, and working with external organizations to improve industry laboratory and quality standards. QA Advisors are required to interface with local laboratory staff, Business unit Product Quality Advisors, Corporate Auditors, and external organizations. Global QA Advisors interact with the Global EMBSI(ExxonMobil Biomedical Sciences, Inc) team to implement the business unit lab assessment program and provide technical consulting support.

Job Role Responsibilities

. Assess whether a laboratory is in compliance with quality control procedures and standards or not.
. Assess both ExxonMobil and third-party contract laboratories against internal as well as industry standards including ISO 17025.
. Conduct assessments at laboratory sites or remotely through desk-top or video audits as required travel requirement is typically 50%.
. Examine laboratory standards, procedures, test methods, and testing equipment for conformance to requirements. Accurately pinpoint issues in documentation, data quality, and performance through the assessment.
. Prepare well written assessment reports documenting the assessment, compliance status, and recommendations for enhancing the quality system.
. Lead assessment preparation, progress, and close-out meetings with staff and management as required. Assist laboratory staff with audit follow-up when required.
. Coordinate with auditing teams and ensure excellent communications between teams and laboratory management.
. Assist in the development of the assessment schedule and plan. Assist in the development of annual budgets for assigned assessment areas.
. Provide professional and technical input for enhancements to data integrity and quality systems.
. Provide quality assurance technical support and consulting to laboratories as required.

Job Requirements

. Strong knowledge of product quality assurance systems and methods including ISO 17025.
. Solid experience with auditing tools such as control charts and statistical methods related to test methods and data.
. ISO 17025 Lead Auditor Certification.
. HUET (Helicopter Underwater Escape Training) Certification, or the ability to complete HUET training course.
. Strong ability to effectively manage working time and schedule.
. Strong attention to detail, analytical, and problem solving ability.
. Exceptional presentation, listening, and communication skills.
. Ability to work effectively with all levels of the organization.
. Able to work effectively as part of a diverse team of auditors and independently.
. Ability to communicate fluently in both oral and written English. Must efficiently write technical reports and effectively present the information related to assessments.
. Strong ability to coach and educate team members and laboratory staff.
. Excellent hearing and vision required for normal assessment conversations, receiving information, and performing inspections.
. Must have the ability to travel to and move about offices and laboratories around the Company.
. Must be computer literate and proficient in commonly available software including MS Word, Excel, Access, and PowerPoint.
. Bachelor's degree with three or more years of internal auditing experience is desirable.
. Oil and Chemical industry laboratory and manufacturing experience
. ASQ(American Society for Quality)certifications are desirable
. Effective communication in languages in addition to English preferred
ExxonMobil does not use recruiting or placement agencies that charge candidates an advance fee of any kind (e.g., placement fees, immigration processing fees, etc.). Follow the to understand more about recruitment scams in the name of ExxonMobil.