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Company: Rieke do Brasil Embalagens Ltda.

Primary Location: Avenida Juvenal Arantes, nº 2500, Galpão 19, Condo, Jundiai, Sao Paolo BRA

Employment Type: Salaried | Full-Time

Function: Quality

Equal Opportunity Employer Minorities/Women/Veterans/Disabled

Main Duties & Responsibilities

Position Summary:

The Quality Analyst evaluates activities at the Brazil plant to confirm that those activities comply with quality standards as well as established policies and procedures to ensure that customers receive product that meets or exceeds their quality requirements.

Primary Duties And Responsibilities

• Identification and reporting of quality data internally and externally.
• Performs a variety of quality control tests on products at various stage of the production process to ensure compliance with quality and reliability standards, with a highlight on metrology.
• Records statistical data.
• Assists in reconciliation and special project research as needed.
• Analyzes data and writes summaries to validate or show deviations from existing standards.
• Recommends modifications to existing, or suggests new standards, methods or procedures.
• Enable effective communications between management and operators.
• Responsible for reviewing and preparing documents for ISO 9001 and ISO 45001 internal audits as well as the timely completion of LPA’s.
• Performs visual and dimensional inspection on all color programs to verify compliance with the customer requirements. Review vendor supplied documentation for accuracy and compliance. Prepare documentation as to acceptance or rejection. Prepare design samples and range boards.
• Assigns and reviews work with quality technicians, training and working effectively with employees from a variety of backgrounds and with different levels and areas of training.
• Ability to communicate effectively in writing to develop and write work procedures, policies, reports, instructions, briefings and other documents.
• Responsible for identifying, segregating, preparing required documents and immediate reporting of all non-conforming materials to appropriate personnel.
• Complete customer QN Investigations by providing QC Manager with pertinent data of the failure modes, clean points, lot traceability, etc.
• Oversee floor QC issues by ensuring the completion of daily firefighting of floor quality issues, decision making for the floor leadership based on established acceptable criteria
• Oversee GP-12 safe launches-training GP-12 inspectors, collecting and analyzing data, training floor leadership, writing inspection reports, overall responsibility to the safe launch efforts.
  
  

• Proficient in reading prints.
• Experience providing Quality Systems training to employees.
• Proficiency in MS Word, Excel, QA application and general math.
• Familiarity with gauge/inspection process.
• Knowledge and use of measuring instruments (caliper, micrometer, etc.)
• Strong communication skills; verbal and written.
• Strong problem solving and analytical skills. (8D, Fishbone, 5 whys)
• Ability to communicate with all levels of the plant to include mentoring, training, and root cause analysis.
• 3 years’ experience in Quality management systems with working knowledge of statistical process controls, preferably in the plastics industry.
• Excels in process, product and system audits.
• Technical writing experience preferred.
• Demonstrated experience leading teams and taking initiative

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Packaging and Containers Manufacturing

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Company Description

At QIMA, we’re on a mission to help our clients make products consumers can trust.

Working with over 30,000 global brands, retailers, manufacturers and food growers, we are on the ground wherever products are made. We help businesses secure every step of their supply chain with quality inspections, supplier audits, certifications, and lab testing, all powered by our intelligent digital platform.

Our team of 5,000 QIMers (and counting) across 40 offices and laboratories, are united in our shared passion for innovation and integrity, and guided by our QIMA values in the decisions we make every day. We believe in the work we do, and in making a positive difference in the world. Does this sound like something you’d like to be a part of?

Our Consumer Goods Division is dedicated to helping brands, retailers and manufacturers worldwide deliver safe, quality and ethically made products to their consumers. Every day at work, our inspectors, auditors, and lab techs use their expertise to help safeguard the products you use every day in your home: from clothes and footwear to toys and baby products, to electronics, appliances, and furniture.

Job Description

As a Quality Control Inspector, you'll be reporting to an Operations Manager and working as a part of our Operations team. At QIMA, the role of Operations is to deliver our industry-leading services to our clients while ensuring that all the work is performed to the QIMA standard of quality. Your role in this will be to:

• Check email daily in order to receive inspection documents and guidelines;
• Attend inspections on time and communicate with supplier in a professional way;
• Perform the inspection of the merchandise according to company procedures. Supervise the stuffing of the containers according to company procedures;
• Fulfill inspection reports according to company procedures and timelines.

• Experience in quality management, especially softlines/ garments/ textiles/ footwear (2 years or more);
• Knowledge of AQL standards, as well as relevant safety and quality regulations;
• Good command of English (spoken and written);
• Great attention to detail and strong professional ethics.

Direct message the job poster from Cipla

Plan and lead the quality control routine operations and stability studies and drive the team to confirm testing as per the GLP guidelines and regulatory requirements and achieve timely release of batches and SRB targets to meet unit OTIF.

Key Accountabilities

I. Plan the quality control routine operations and stability studies to ensure timely completion of stability studies and smooth functioning of release activity

• Monitor the commitment dates for release of RM, PM, FP & water analysis and process/cleaning validation section by conducting performance dialogues and handshake

• Review the plans prepared and monitor timely execution of activities in all the shifts to avoid delays

• Review the monthly planner and production plans to ensure timely availability of required resources and ensure no sample is overdue

II. Monitor the execution of all routine quality control operation and stability studies to ensure timely delivery and meet regulatory requirements and cGMP, GLP guidelines

• Monitor routine/stability operations closely and ensure that all necessary SOPs are followed by the team

• Provide technical guidance related to troubleshooting in chromatography, experimentation design etc. to minimize non-conformances

• Monitor timely implementation of new updates in specifications and QCPs to meet compliance

• Perform online review of reports generated to ensure zero data integrity issues in Lab

• Monitor sample charging and sample pull-out as per schedule

• Monitor reserved samples storage and destruction as per schedule and perform UD release

• Monitor the stability chamber daily for excursions and other related issues

III. Drive the investigation of the batch for non-conformance and ensure its closure within the timelines defined in SOPs to facilitate smooth operations

• Evaluate root cause analysis in case of OOS, OOT, incidences and rejection and propose CAPAs

• Investigate the stability chamber excursions and propose CAPAs

• Ensure that all non-conformances are routed through proper channel and are investigated as per SOP

• Communicate with respective QC/QA heads for compliance and ensure timely closure of CAPAs by tracking in SmartSolve

IV. Monitor completion of stability studies as per protocol/schedule to avoid delays in product launch

• Perform analysis for stability samples without any errors as per schedule

• Ensure timely completion of ANDA samples testing and submission of data by verifying it with ANDA schedule

• Plan the routine/stability activities by coordinating with ADL/R&D about dates of product dossier filing

• Resolve analytical and product related issues by escalating to ADL, R&D and transfer unit

V. Provide technical guidance to the team w.r.t batch release and stability studies and evaluate their performance to ensure team development and improved lab efficiency

• Identify the training needs of employees based on the updates in the pharmacopeial guidelines

• Monitor the training imparted on laboratory techniques, quality control procedures and principles of cGMP & GLP

• Monitor the productivity of all the teams in the section by reviewing %SLA and %NC rates

• Ensure the completion of training and qualification of analyst by taking feedback and timely reviewing his work

Skills & Knowledge

• 9+ years of experience in quality control function of a pharmaceutical organisation. At least 2-3 years of experience leading a team

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Pharmaceutical Manufacturing and Retail Pharmacies

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Quality Assurance Analyst

**This is an administrative, non-technical position focused on document review and proofreading.**

LegalSight is a dynamic, innovative, and growing organization. We like to have fun while taking our work very seriously. Quality control is central to LegalSight and a great quality team member is dedicated with a high degree of attention to detail!

The Quality Assurance Analyst will provide quality assessments of language translation projects in order to ensure we meet our client’s quality standards.

Key Elements of the Role:

• This is a fully remote position.
• Working hours during the 30-day training period will be Monday - Friday 10:00PM - 6:00PM Brazil time. Once training is complete, working hours will change to Monday - Friday 10:00AM - 6:00PM Brazil time .
• Fluency in spoken and written English is required for this role as you would be collaborating with and supporting team members internationally.

Key Responsibilities:

• Complete quality review of translations.
• Collaborate with Project Management Team to clarify project parameters.
• Communicate effectively with vendors world-wide in order to reconcile any found errors.
• Implement process improvements using available technology solutions.

Essential Skills:

• Highly-focused, detail-oriented, and client-centric mindset
• Capable of setting and meeting deadlines
• Ability to manage time effectively
• Excellent communication skills
• Proven problem-solving skills
• Ability to work well in both independent and highly collaborative settings
• Ability to excel in fast-paced work environment
• High degree of proficiency in relevant computer skills (MS Office)

This is an administrative, non-technical position focused on document review and proofreading. LegalSight is a dynamic, innovative, and growing organization. We like to have fun while taking our work very seriously. Quality control is central to LegalSight and a great quality team member is dedicated with a high degree of attention to detail!

The Quality Assurance Analyst will provide quality assessments of language translation projects in order to ensure we meet our client’s quality standards.

• This is a fully remote position.
• Working hours during the 30-day training period will be Monday - Friday 10:00PM - 6:00PM Brazil time. Once training is complete, working hours will change to Monday - Friday 10:00AM - 6:00PM Brazil time.
• Fluency in spoken and written English is required for this role as you would be collaborating with and supporting team members internationally.

• Complete quality review of translations.
• Collaborate with Project Management Team to clarify project parameters.
• Communicate effectively with vendors world-wide in order to reconcile any found errors.
• Implement process improvements using available technology solutions.
• Highly-focused, detail-oriented, and client-centric mindset.
• Capable of setting and meeting deadlines.
• Ability to manage time effectively.
• Proven problem-solving skills.
• Ability to work well in both independent and highly collaborative settings.
• Ability to excel in fast-paced work environment.
• High degree of proficiency in relevant computer skills (MS Office).

• Entry level

• Full-time

• Administrative and Writing/Editing

• Legal Services and Translation and Localization

Korean Quality C ontrol R eviewer

The Language Doctors, Inc. is a US-based l i nguistic services provider known for its commitment to quality and precision. We are currently seeking a detail-oriented and bilingual Korean Quality Control Reviewer to join our team. This role is ideal for professionals fluent in Japanese and English with a strong eye for linguistic accuracy and consistency.

Key Responsibilities:

• Monitor overall document quality to ensure adherence to client-specific and internal standards throughout the review process.

• Review linguistic content to verify grammatical accuracy, appropriate terminology , and alignment with style guides and tone requirements.

• Check formatting and layout to ensure documents follow template specifications, visual consistency, and structural completeness.

• Suggest process improvements and participate in root-cause analysis when errors are detected.

• Collaborate with team members to communicate findings and escalate quality concerns as needed.

• Ensure projects are delivered within timelines while maintaining high quality.
  

Qualifications :

• Native or near-native fluency in Korean , with strong command of written and verbal English (minimum B2 CEFR level).

• Minimum 1–2 years of experience in Quality Assurance or document review, preferably in the medical or life sciences fields.

• Demonstrated attention to detail and ability to analyse complex documents for consistency and quality.

• Proficient in Microsoft Word and Excel , including formatting, comments, and revision tools.

• Strong organizational and time management skills with the ability to meet deadlines independently.

Preferred Skills:

• Experience reviewing Korean handwrit ten documents and translated texts

• Background in transcription, documentation, or translation QA

Technical Requirements :

• Computer with 8 GB RAM or higher

• Intel i5 (5th gen or newer) or equivalent processor

• Microsoft Office 2019 or later

• Reliable internet connection ( 50 Mbps minimum )

Available Schedules:

• Monday to Friday | 9 :00 AM to 5 : 30 PM EST
• Monday to Friday | 0 2 :00 PM to 10: 30 PM EST

The Language Doctors, Inc. is an equal-opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race,color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Visit our website at to learn more about us.

Japanese Quality C ontrol R eviewer

The Language Doctors, Inc. is a US-based l i nguistic services provider known for its commitment to quality and precision. We are currently seeking a detail-oriented and bilingual Japanese Quality Control Reviewer to join our team. This role is ideal for professionals fluent in Japanese and English with a strong eye for linguistic accuracy and consistency.

Key Responsibilities:

• Monitor overall document quality to ensure adherence to client-specific and internal standards throughout the review process.

• Review linguistic content to verify grammatical accuracy, appropriate terminology , and alignment with style guides and tone requirements.

• Check formatting and layout to ensure documents follow template specifications, visual consistency, and structural completeness.

• Suggest process improvements and participate in root-cause analysis when errors are detected.

• Collaborate with team members to communicate findings and escalate quality concerns as needed.

• Ensure projects are delivered within timelines while maintaining high quality.
  

Qualifications :

• Native or near-native fluency in Japanese , with strong command of written and verbal English (minimum B2 CEFR level).

• Minimum 1–2 years of experience in Quality Assurance or document review, preferably in the medical or life sciences fields.

• Demonstrated attention to detail and ability to analyse complex documents for consistency and quality.

• Proficient in Microsoft Word and Excel , including formatting, comments, and revision tools.

• Strong organizational and time management skills with the ability to meet deadlines independently.

Preferred Skills:

• Experience reviewing Japanese handwrit ten documents and translated texts

• Background in transcription, documentation, or translation QA

Technical Requirements :

• Computer with 8 GB RAM or higher

• Intel i5 (5th gen or newer) or equivalent processor

• Microsoft Office 2019 or later

• Reliable internet connection ( 50 Mbps minimum )

Available Schedules:

• Monday to Friday | 9 :00 AM to 5 : 30 PM EST
• Monday to Friday | 0 2 :00 PM to 10: 30 PM EST
  
• Monday to Friday| 10:00 PM to 06:30 AM EST

The Language Doctors, Inc. is an equal-opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race,color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Visit our website at to learn more about us.

1 day ago Be among the first 25 applicants

Direct message the job poster from The Language Doctors

The Language Doctors, Inc. is a US-based linguistic services provider known for its commitment to quality and precision. We are currently seeking a detail-oriented and bilingual Japanese Quality Control Reviewer to join our team.

This role is ideal for professionals fluent in Japanese and English with a strong eye for linguistic accuracy and consistency.

Key Responsibilities:

• Monitor overall document quality to ensure adherence to client-specific and internal standards throughout the review process.
• Review linguistic content to verify grammatical accuracy, appropriate terminology, and alignment with style guides and tone requirements.
• Check formatting and layout to ensure documents follow template specifications, visual consistency, and structural completeness.
• Suggest process improvements and participate in root-cause analysis when errors are detected.
• Collaborate with team members to communicate findings and escalate quality concerns as needed.
• Ensure projects are delivered within timelines while maintaining high quality.

Qualifications:

• Native or near-native fluency in Japanese, with excellent written and verbal English skills (minimum B2 CEFR level; C1 preferred).
• At least 1–2 years of professional experience in translation, localization, medical transcription, or linguistic QA, especially within the life sciences, healthcare, or pharmaceutical industries.
• Proven experience working with bilingual or multilingual documentation (source and target language).
• Demonstrated ability to review and correct terminology, ensure consistency across translations, and apply style guides.
• Proficient in Microsoft Word and Excel, including use of comments, tracked changes, and formatting tools.
• Excellent attention to detail, with a methodical and analytical approach to linguistic accuracy and medical terminology.
• Strong time management skills and ability to meet tight deadlines independently.

Preferred Skills:

• Hands-on experience in quality assurance for translated content, especially medical documents.
• Background in transcription QA, linguistic validation, or post-editing of machine translations.
• Experience reviewing Japanese handwritten medical records is a strong advantage.

Technical Requirements:

• Computer with 8GB RAM or higher
• Intel i5 (5th gen or newer) or equivalent processor
• Microsoft Office 2019 or later
• Reliable internet connection (50 Mbps minimum)

Available Schedules:

• Monday to Friday | 9:00 AM to 5:30 PM EST
• Monday to Friday | 2:00 PM to 10:30 PM EST
• Monday to Friday | 10:00 PM to 06:30 AM EST

The Language Doctors, Inc. is an equal-opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Visit our website at to learn more about us.

• Seniority level Entry level

• Employment type Full-time

• Job function Administrative
• Industries Translation and Localization

Referrals increase your chances of interviewing at The Language Doctors by 2x

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.